UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-Q
☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE
SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended March 31, 2021
or
☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE
SECURITIES EXCHANGE ACT OF 1934
Commission file number: 333-216054
AVRA MEDICAL ROBOTICS, INC.
(Exact name of registrant as specified in its charter)
Florida |
|
47-3478854 |
(State
or Other Jurisdiction of |
|
(I.R.S.
Employer |
Incorporation
or Organization) |
|
Identification
No.) |
3259 Progress Drive,
Suite 112A, Orlando, FL 32826
(Address of Principal Executive Offices)
(407)
956-2250
(Registrant’s telephone number, including area code)
(Former name, former address and former fiscal year, if changed
since last report)
Securities registered pursuant to Section 12(b) of the
Act:
Title
of each class |
|
Trading
Symbol(s) |
|
Name
of each exchange on
which registered |
None |
|
N/A |
|
N/A |
Indicate by check mark whether the registrant has submitted
electronically every Interactive Data File required to be submitted
pursuant to Rule 405 of Regulation S-T during the preceding 12
months (or for such shorter period that the Registrant was required
to submit such files.) Yes ☐ No ☒
Indicate by check mark whether the registrant is a large
accelerated filer, an accelerated filer, a non-accelerated filer, a
smaller reporting company or an emerging growth company. See the
definitions of “accelerated filer”, “large accelerated filer,”
“smaller reporting company” and “emerging growth company” in
Rule 12b-2 of the Exchange Act.
Large
Accelerated Filer |
☐ |
Accelerated
Filer |
☐ |
Non-Accelerated
Filer |
☒ |
Smaller
reporting company |
☒ |
|
Emerging
growth company |
☒ |
If an emerging growth company, indicate by check mark if the
registrant has elected not to use the extended transition period
for complying with any new or revised financial accounting
standards provided pursuant to Section 13(a) of the Exchange
Act. ☐
Indicate by check mark whether the registrant is a shell company
(as defined in Rule 12b-2 of the Exchange Act).
Yes ☐ No ☒
There were 39,197,099 shares of common stock, $0.0001 par value of
the Registrant issued and outstanding as of November 1, 2022.
TABLE OF CONTENTS
PART I – FINANCIAL
INFORMATION
Item 1. Financial Statements.
AVRA MEDICAL ROBOTICS, INC.
CONDENSED BALANCE SHEETS
AS ON MARCH 31, 2021
(Unaudited)
|
|
March 31,
2021 |
|
|
December 31,
2020 |
|
|
|
|
|
|
|
|
ASSETS |
|
|
|
|
|
|
CURRENT ASSETS: |
|
|
|
|
|
|
Cash and cash equivalents |
|
$ |
316,813 |
|
|
$ |
160,709 |
|
Other prepaid expenses and deposit |
|
$ |
2,291 |
|
|
$ |
2,290 |
|
Total
Current Assets |
|
$ |
319,104 |
|
|
$ |
162,999 |
|
|
|
|
|
|
|
|
|
|
EQUIPMENT: |
|
|
|
|
|
|
|
|
Equipment |
|
$ |
98,592 |
|
|
$ |
98,592 |
|
Accumulated depreciation |
|
$ |
(66,602 |
) |
|
$ |
(60,385 |
) |
Total
Equipment, net |
|
$ |
31,990 |
|
|
|
38,207 |
|
|
|
|
|
|
|
|
|
|
INVESTMENT: |
|
|
|
|
|
|
|
|
Investment in Avra
Air LLC |
|
$ |
115,542 |
|
|
$ |
115,542 |
|
|
|
|
|
|
|
|
|
|
OTHER
ASSETS: |
|
|
|
|
|
|
|
|
Website |
|
$ |
36,122 |
|
|
$ |
36,122 |
|
Accumulated amortization |
|
$ |
(36,122 |
) |
|
$ |
(35,000 |
) |
Total Other Assets, net |
|
$ |
-
|
|
|
$ |
1,122 |
|
|
|
|
|
|
|
|
|
|
TOTAL ASSETS |
|
$ |
466,635 |
|
|
$ |
317,870 |
|
|
|
|
|
|
|
|
|
|
LIABILITIES AND STOCKHOLDERS’ DEFICIT |
|
|
|
|
|
|
|
|
CURRENT LIABILITIES: |
|
|
|
|
|
|
|
|
Accounts
payable |
|
$ |
103,440 |
|
|
$ |
131,719 |
|
Accrued
compensation |
|
|
|
|
|
|
|
|
Accrued
expenses |
|
$ |
927,700 |
|
|
$ |
860,200 |
|
Notes payable - related party |
|
$ |
195,000 |
|
|
$ |
195,000 |
|
Total Current
Liabilities |
|
$ |
1,226,140 |
|
|
$ |
1,186,919 |
|
|
|
|
|
|
|
|
|
|
Commitments and
contingencies (see Note 8) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
STOCKHOLDER’S DEFICIT: |
|
|
|
|
|
|
|
|
Preferred stock, 5,000,000 shares authorized, $.0001 par value,
none
issued or outstanding |
|
|
-
|
|
|
|
-
|
|
|
|
|
|
|
|
|
|
|
Common
stock, 100,000,000 shares authorized, $.0001 par value, 26,746,971
and 25,721,971 issued and outstanding at March 31, 2021, and
December 31, 2020 respectively |
|
$ |
2,675 |
|
|
$ |
2,572 |
|
Common stock
liability, 345,480 and 289,697 shares, $.0001 par value at March
31, 2021 and December 31, 2020, respectively |
|
$ |
151,434 |
|
|
$ |
100,925 |
|
Additional
paid-in capital |
|
$ |
6,380,190 |
|
|
$ |
6,021,201 |
|
Accumulated Deficit |
|
$ |
(7,293,803 |
) |
|
$ |
(6,993,747 |
) |
Total Stockholders’ Deficit |
|
$ |
(759,504 |
) |
|
$ |
(869,049 |
) |
|
|
|
|
|
|
|
|
|
TOTAL
LIABILITIES AND STOCKHOLDER’S DEFICIT |
|
$ |
466,635 |
|
|
$ |
317,870 |
|
See accompanying notes to unaudited Condensed Financial
Statements.
AVRA MEDICAL ROBOTICS, INC.
CONDENSED STATEMENTS OF OPERATIONS
FOR THE QUARTERLY PERIOD ENDED MARCH
(Unaudited)
|
|
2021 |
|
|
2020 |
|
|
|
|
|
|
|
|
Revenues |
|
$ |
-
|
|
|
$ |
-
|
|
|
|
|
|
|
|
|
|
|
OPERATING EXPENSES |
|
|
|
|
|
|
|
|
Research and Development |
|
$ |
- |
|
|
$ |
2,000 |
|
Compensation
Expense |
|
$ |
219,600 |
|
|
$ |
223,944 |
|
General and Administrative |
|
$ |
80,478 |
|
|
$ |
80,727 |
|
Total Operating Expenses |
|
$ |
300,078 |
|
|
$ |
306,671 |
|
|
|
|
|
|
|
|
|
|
OTHER INCOME AND (EXPENSES) |
|
|
|
|
|
|
|
|
Interest
Earned |
|
$ |
22 |
|
|
$ |
- |
|
Interest Expense |
|
$ |
- |
|
|
$ |
(344 |
) |
Total Other Income and (Expenses), net |
|
$ |
22 |
|
|
$ |
(344 |
) |
|
|
|
|
|
|
|
|
|
Loss before Income Taxes |
|
$ |
(300,056 |
) |
|
$ |
(307,015 |
) |
|
|
|
|
|
|
|
|
|
Provision for
Income Taxes |
|
$ |
-
|
|
|
$ |
-
|
|
|
|
|
|
|
|
|
|
|
NET LOSS |
|
$ |
(300,056 |
) |
|
$ |
(307,015 |
) |
|
|
|
|
|
|
|
|
|
Loss per common share - basic and diluted
|
|
$ |
(0.01 |
) |
|
$ |
(0.01 |
) |
|
|
|
|
|
|
|
|
|
Weighted average common shares outstanding |
|
|
|
|
|
|
|
|
-
basic and diluted
|
|
|
26,261,471 |
|
|
|
22,976,445 |
|
See accompanying notes to unaudited Condensed Financial
Statements.
AVRA MEDICAL ROBOTICS, INC.
CONDENSED STATEMENT OF STOCKHOLDERS’ (DEFICIT)
FOR THE QUARTERLY PERIOD ENDED MARCH 31, 2021 and 2020
(Unaudited)
|
|
Common Stock |
|
|
Common Stock to be Issued |
|
|
Additional
Paid-In |
|
|
Accumulated |
|
|
Total
Stockholders’ |
|
|
|
Number |
|
|
Amount |
|
|
Number |
|
|
Amount |
|
|
Capital |
|
|
Deficit |
|
|
Deficit |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
BALANCE AT DECEMBER 31, 2020 |
|
|
25,721,971 |
|
|
$ |
2,572 |
|
|
|
289,697 |
|
|
$ |
100,925 |
|
|
$ |
6,021,201 |
|
|
$ |
(6,993,747 |
) |
|
$ |
(869,049 |
) |
Stock based compensation expense |
|
|
-
|
|
|
|
-
|
|
|
|
-
|
|
|
|
-
|
|
|
$ |
37,674 |
|
|
|
-
|
|
|
$ |
37,674 |
|
Stock issued for services |
|
|
60,000 |
|
|
$ |
6 |
|
|
|
-
|
|
|
|
-
|
|
|
$ |
181,136 |
|
|
|
-
|
|
|
$ |
181,142 |
|
Security Offerings |
|
|
940,000 |
|
|
$ |
94 |
|
|
|
|
|
|
|
|
|
|
$ |
117,964 |
|
|
|
-
|
|
|
$ |
118,058 |
|
Common stock issuable for services |
|
|
|
|
|
|
|
|
|
|
80,783 |
|
|
$ |
72,726 |
|
|
|
- |
|
|
|
- |
|
|
$ |
72,726 |
|
Common stock issued |
|
|
25,000 |
|
|
$ |
3 |
|
|
|
(25,000 |
) |
|
$ |
(22,218 |
) |
|
$ |
22,215 |
|
|
|
-
|
|
|
|
-
|
|
Net loss |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
$ |
(300,056 |
) |
|
$ |
(300,056 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
BALANCE AT MARCH 31, 2021 |
|
|
26,746,971 |
|
|
$ |
2,675 |
|
|
|
345,480 |
|
|
$ |
151,434 |
|
|
$ |
6,380,190 |
|
|
$ |
(7,293,803 |
) |
|
$ |
(759,504 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
BALANCE AT
DECEMBER 31, 2019 |
|
|
21,857,218 |
|
|
$ |
2,186 |
|
|
|
128,909 |
|
|
$ |
254,564 |
|
|
$ |
4,549,058 |
|
|
$ |
(5,869,066 |
) |
|
$ |
(1,063,258 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Stock based compensation expense |
|
|
-
|
|
|
|
-
|
|
|
|
-
|
|
|
|
-
|
|
|
$ |
126,059 |
|
|
|
-
|
|
|
$ |
126,059 |
|
Stock issued for services |
|
|
1,013,334 |
|
|
$ |
101 |
|
|
|
-
|
|
|
|
-
|
|
|
$ |
119,899 |
|
|
|
-
|
|
|
$ |
120,000 |
|
Stock warrants |
|
|
122,200 |
|
|
$ |
12 |
|
|
|
-
|
|
|
|
-
|
|
|
$ |
203,832 |
|
|
|
-
|
|
|
$ |
203,844 |
|
Common stock issuable for services |
|
|
|
|
|
|
|
|
|
|
(13,901 |
) |
|
|
(170,938 |
) |
|
|
-
|
|
|
|
-
|
|
|
$ |
(170,938 |
) |
Net loss |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
$ |
(307,015 |
) |
|
$ |
(307,015 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
BALANCE AT MARCH 31, 2020 |
|
|
22,992,752 |
|
|
$ |
2,299 |
|
|
|
115,008 |
|
|
$ |
83,626 |
|
|
$ |
4,998,848 |
|
|
$ |
(6,176,081 |
) |
|
$ |
(1,091,308 |
) |
See accompanying notes to unaudited Condensed Financial
Statements.
AVRA MEDICAL ROBOTICS, INC.
CONDENSED STATEMENTS OF CASH FLOWS
FOR THE QUARTERLY PERIOD ENDED MARCH
(Unaudited)
|
|
2021 |
|
|
2020 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
CASH FLOWS FROM OPERATING ACTIVITIES: |
|
|
|
|
|
|
Net Loss |
|
$ |
(300,056 |
) |
|
$ |
(307,015 |
) |
|
|
|
|
|
|
|
|
|
Adjustments to reconcile net loss to net cash used in operating
activities: |
|
|
|
|
|
|
|
|
Depreciation and amortization expense |
|
$ |
7,339 |
|
|
$ |
9,358 |
|
Stock
compensation expense |
|
$ |
174,600 |
|
|
$ |
178,945 |
|
Non-cash interest |
|
$ |
-
|
|
|
$ |
-
|
|
Changes in operating assets and liabilities: |
|
|
|
|
|
|
|
|
Prepaid
expenses |
|
$ |
-
|
|
|
$ |
4,000 |
|
Accounts payable and accrued expenses |
|
$ |
39,220 |
|
|
$ |
64,358 |
|
Net Cash Used in Operating Activities |
|
$ |
(78,896 |
) |
|
$ |
(50,354 |
) |
|
|
|
|
|
|
|
|
|
INVESTING ACTIVITIES: |
|
|
|
|
|
|
|
|
Equipment acquisition |
|
$ |
-
|
|
|
$ |
(4,000 |
) |
Net Cash Used in Investing Activities |
|
$ |
-
|
|
|
$ |
(4,000 |
) |
|
|
|
|
|
|
|
|
|
FINANCING ACTIVITIES: |
|
|
|
|
|
|
|
|
Proceeds from
securities offering |
|
$ |
235,000 |
|
|
$ |
-
|
|
Proceeds from related party |
|
$ |
-
|
|
|
$ |
101,000 |
|
Proceeds from promissory notes |
|
$ |
-
|
|
|
$ |
(65,000 |
) |
Net Cash Provided by Financing Activities |
|
$ |
235,000 |
|
|
$ |
36,000 |
|
|
|
|
|
|
|
|
|
|
INCREASE (DECREASE) IN CASH AND CASH EQUIVALENTS |
|
$ |
156,104 |
|
|
$ |
(18,354 |
) |
|
|
|
|
|
|
|
|
|
CASH AND CASH EQUIVALENTS - BEGINNING OF PERIOD |
|
$ |
160,709 |
|
|
$ |
28,474 |
|
|
|
|
|
|
|
|
|
|
CASH AND CASH EQUIVALENTS - END OF PERIOD |
|
$ |
316,813 |
|
|
$ |
10,120 |
|
|
|
|
|
|
|
|
|
|
Supplemental information of non-cash investing and financing
activities: |
|
|
|
|
|
|
|
|
Non-cash
investing activities: |
|
|
|
|
|
|
|
|
Cash paid for interest |
|
$ |
-
|
|
|
$ |
344 |
|
Cash received for interest |
|
$ |
22 |
|
|
$ |
-
|
|
|
|
|
|
|
|
|
|
|
Non-cash
financing activities: |
|
|
|
|
|
|
|
|
Related party note payable converted into common stock |
|
$ |
-
|
|
|
$ |
100,000 |
|
Promissory note converted into common stock |
|
$ |
-
|
|
|
$ |
20,000 |
|
Reduction of account payable and equipment |
|
$ |
4,743 |
|
|
$ |
25000 |
|
See accompanying notes to unaudited Condensed Financial
Statements.
AVRA MEDICAL ROBOTICS, INC.
NOTES TO FINANCIAL STATEMENTS
NOTE 1 – COMPANY AND BASIS OF PRESENTATION
Organization
AVRA Medical Robotics, Inc. (the “Company” or “AVRA”) was
incorporated as AVRA Surgical Microsystems, Inc. in the State of
Florida on February 4, 2015. Effective November 5, 2015, the
Company’s corporate name was changed to AVRA Medical Robotics, Inc.
The Company was established to develop advanced medical surgical
devices. The Company is structured to invest in four principal
areas – surgical robotic systems, surgical tools, implantable
devices and surgical robotic training.
The significant accounting policies of AVRA were described in Note
1 to the audited financial statements included in the Company’s
2020 Annual Report on Form 10-K (“2020 Form 10-K”). There have been
no significant changes in the Company’s significant accounting
policies for the quarterly period ended March 31, 2021.
Basis of
Presentation
The accompanying unaudited condensed financial statements of the
Company have been prepared in conformity with accounting principles
generally accepted in the United States (“GAAP”) for interim
financial information and in accordance with the rules and
regulations of the Securities and Exchange Commission.
Therefore, they do not include all information and footnotes
normally included in annual consolidated financial statements and
should be read in conjunction with the consolidated financial
statements and notes thereto included in the 2020 Form 10-K for the
year ended December 31, 2020. In the opinion of the Company’s
management, the accompanying unaudited condensed financial
statements contain all the adjustments necessary (consisting only
of normal recurring accruals) to present the financial position of
the Company as of March 31, 2021 and the results of operations and
cash flows for the periods presented. The results of operations for
the quarterly period ended March 31, 2021 are not necessarily
indicative of the operating results for the full fiscal year or any
future period.
Going Concern
The accompanying financial statements have been prepared assuming
the continuation of the Company as a going concern. At March 31,
2021, the Company’s stockholders’ deficit was $759,504 which raises
substantial doubt about the Company. The Company has not yet
established an ongoing source of revenues sufficient to cover its
operating costs and is dependent on debt and equity financing to
fund its operations. Management of the Company is making efforts to
raise additional funding until a registration statement relating to
an equity funding facility is in effect. While management of the
Company believes that it will be successful in its capital
formation and planned operating activities, there can be no
assurance that the Company will be able to raise additional equity
capital or be successful in the development and commercialization
of the products it develops or initiates collaboration agreements
thereon. The accompanying financial statements do not include any
adjustments to reflect the possible future effects on the
recoverability and classification of assets or the amounts and
classification of liabilities that may result from the possible
inability of the Company to continue as a going concern.
NOTE 2 - SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Estimates
The preparation of financial statements in conformity with GAAP
requires management to make estimates and assumptions that affect
the reported amounts of assets, liabilities and expenses. The
Company regularly evaluates estimates and assumptions that affect
the reported amounts of assets and liabilities and disclosure of
contingent assets and liabilities at the date of the financial
statements and the reported amounts of revenues and expenses during
the reporting period. Actual results could differ from those
estimates made by management.
Cash and Cash
Equivalents
The Company considers all cash on hand, cash accounts not subject
to withdrawal restrictions or penalties, and all highly liquid debt
instruments purchased with a maturity of three months or less to be
cash and cash equivalents.
Concentration of Credit
Risk
Financial instruments that potentially subject the Company to
concentrations of credit risk consist principally of cash. The
Company maintains its principal cash balance in a financial
institution. These balances are insured by the Federal Deposit
Insurance Corporation (“FDIC”) up to $250,000. At March 31, 2021
and 2020, $54,314 and $0 were in excess of the FDIC insured limit
respectively.
Revenue
Recognition
In May 2014, the Financial Accounting Standards Board (“FASB”)
issued Accounting Standards Update (“ASU”) No. 2014-09, Revenue
from Contracts with Customers (Topic 606). The ASU and all
subsequently issued clarifying ASUs replaced most existing revenue
recognition guidance in U.S. GAAP. The ASU also required expanded
disclosures relating to the nature amount, timing, and uncertainty
of revenue and cash flows arising from contracts with customers.
The Company adopted the new standard effective January 1, 2018, the
first day of the Company’s fiscal year. For these reasons, the
adoption of this ASU did not have a significant impact on the
Company’s financial statements
Effective January 1, 2018, the Company adopted guidance issued by
the FASB regarding recognizing revenue from contracts with
customers. The revenue recognition policies as enumerated below
reflect the Company’s accounting policies effective January 1,
2018, which did not have a materially different financial statement
result than what the results would have been under the previous
accounting policies for revenue recognition.
Equipment
Equipment is recorded at cost and depreciated using the
straight-line method at rates determined to estimate the useful
lives of the assets. The annual rates used in calculating
depreciation is as follows:
Equipment -5 years straight-line
Intangibles
Intangible assets continue to be subject to amortization, and any
impairment is determined in accordance with ASC 360, “Property,
Plant, and Equipment,” intangible assets are stated at historical
cost and amortized over their estimated useful lives. The Company
uses a straight-line method of amortization, unless a method that
better reflects the pattern in which the economic benefits of the
intangible asset are consumed or otherwise used up can be reliably
determined
The Company purchased existing Intellectual Property from the
University of Central Florida. Management regularly assesses the
carrying value of the intellectual property to determine if there
has been any diminution of value.
Website
Website is recorded at cost and amortized using the straight-line
method over its estimated life of 3 years.
Long-lived
Assets
In accordance with ASC 360, “Property Plant and Equipment”,
the Company tests long-lived assets or asset groups for
recoverability when events or changes in circumstances indicate
that their carrying amount may not be recoverable. Circumstances
which could trigger a review include, but are not limited to :
significant decreases in the market price of the asset; significant
adverse changes in the business climate or legal factors;
accumulation of costs significantly in excess of the amount
originally expected for the acquisition or construction of the
asset; current cash flow or operating losses combined with a
history of losses or a forecast of continuing losses associated
with the use of the asset and current expectation that the asset
will more than likely not be sold or disposed significantly before
the end of its estimated useful life. Recoverability is assessed
based on the carrying amount of the asset and its fair value which
is generally determined based on the sum of the discounted cash
flows expected to result from the use and the eventual disposal of
the asset, as well as specific appraisal in certain circumstances.
An impairment loss is recognized when the carrying amount is not
recoverable and exceeds fair value.
Stock Compensation
Expense
The Company accounts for equity instruments issued in exchange for
the receipt of goods or services from other than employees in
accordance with Accounting Standards Codification (“ASC”) Topic
505, “Equity.” Costs are measured at the estimated fair market
value of the consideration received or the estimated fair value of
the equity instruments issued, whichever is more reliably
measurable. The value of equity instruments issued for
consideration other than employee services is determined on the
earlier of a performance commitment or completion of performance by
the provider of goods or services as defined by ASC Topic 505.
Income Taxes
The Company accounts for income taxes pursuant to ASC Topic 740
“Income Taxes.” Under ASC Topic 740, deferred tax assets and
liabilities are determined based on temporary differences between
the bases of certain assets and liabilities for income tax and
financial reporting purposes. The deferred tax assets and
liabilities are classified according to the financial statement
classification of the assets and liabilities generating the
differences. A valuation allowance is recorded when it is more
likely than not that some or all of the deferred tax assets will
not be realized.
The Company applies the provisions of ASC Topic 740-10-05
“Accounting for Uncertainty in Income Taxes.” The ASC
clarifies the accounting for uncertainty in income taxes recognized
in an enterprise’s financial statements. The ASC prescribes a
recognition threshold and measurement attribute for the financial
statement recognition and measurement of a tax position taken or
expected to be taken in a tax return. The ASC provides guidance on
de-recognition, classification, interest and penalties, accounting
in interim periods, disclosure and transition.
Basic and Diluted Loss per
Share
In accordance with ASC Topic 260 “Earnings Per
Share,” basic loss per common share is computed by
dividing net loss available to common stockholders by the weighted
average number of common shares outstanding during the period.
Diluted loss per common share gives effect to dilutive convertible
securities, options, warrants and other potential common stock
outstanding during the period, only in periods in which such effect
is dilutive. The Company has stock options, warrants, and
convertible promissory notes that may be converted to outstanding
potential common shares.
Research and Development
Costs
In accordance with ASC Topic 730 “Research and Development”, with
the exception of intellectual property that is purchased from
another enterprise and have alternative future use, research and
development expenses are charged to operations as incurred.
Fair Value of Financial
Instruments
Our financial instruments consist principally of accounts
receivable, amounts due to related parties and promissory notes
payable. The carrying amounts of cash and cash equivalents and
promissory notes approximate fair value because of the short-term
nature of these items.
Recent Accounting Pronouncements
Compensation—Stock
Compensation
In May 2017, the FASB issued ASU 2017-09, “Compensation—Stock
Compensation (Topic 718): Scope of Modification Accounting,” that
provides guidance about which changes to the terms or conditions of
a share-based payment award require an entity to apply modification
accounting. The new guidance became effective for the Company on
January 1, 2018 and was applied on a prospective basis, as
required. The adoption of this standard did not have an impact on
the financial statements or the related disclosures.
Leases
In February 2016, the FASB issued ASU 2016-02, “Leases (Topic 842)”
(“ASU 2016-02”). The FASB issued ASU 2016-02 to increase
transparency and comparability among organizations recognizing
lease assets and lease liabilities on the balance sheet and
disclosing key information about leasing arrangements. Under ASU
2016-02, lessors will account for leases using an approach that is
substantially equivalent to existing GAAP for sales-type leases,
direct financing leases and operating leases. Unlike current
guidance, however, a lease with collectability uncertainties may be
classified as a sales-type lease. If collectability of lease
payments, plus any amount necessary to satisfy a lessee residual
value guarantee, is not probable, lease payments received will be
recognized as a deposit liability and the underlying assets will
not be derecognized until collectability of the remaining amounts
becomes probable. ASU 2016-02 is effective for interim and annual
periods beginning after December 15, 2018, with early adoption
permitted, and must be adopted using a modified retrospective
transition. The Company did not adopt the standard effective
January 1, 2019, utilizing the lessor practical expedient. On
November 15, 2019, the FASB issued ASU 2019-10 which amended the
effective dates for ASC 842, to give implementation relief. Under
the FASB’s new framework, two “buckets” were defined, bucket 1
includes public companies that are SEC filers but excludes “Small
Reporting Companies” (SRC’s). Bucket 2 includes all other entities,
including SRC’s. Bucket 2 entities have to apply ASC 842 for fiscal
years beginning after December 15, 2020, and interim periods within
fiscal years beginning after December 15, 2021.
NOTE 3 – NOTES PAYABLE – RELATED PARTY
On December 31, 2018, the Company borrowed $15,000 under a
non-interest bearing promissory note from a related party. The note
matured on December 31, 2019 and was extended to December 31,
2020.
On February 6, 2019, the Company borrowed from its CEO, $17,500
under a non-interest bearing promissory note which matures on
February 6, 2020 and was extended to December 31, 2020.
On May 8, 2019, the Company borrowed from its CEO, $25,000 under a
non-interest bearing promissory note which matures on May 8, 2020
and was extended to December 31, 2020.
On May 29, 2019, the Company borrowed from its CEO, $25,000 under a
non-interest bearing promissory note which matures on May 29, 2020
and was extended to December 31, 2020.
On June 26, 2019, the Company borrowed from its CEO, $40,000 under
a non-interest bearing promissory note which matures on June 26,
2020 and was extended to December 31, 2020.
On July 19, 2019, the Company borrowed from its CEO, $50,000 under
a non-interest bearing promissory note which matures on July 19,
2020 and was extended to December 31, 2020.
On October 11, 2019, the Company borrowed from its CEO, $30,000
under a non-interest bearing promissory note which matures on March
11, 2020 and was extended to December 31, 2020.
On November 14, 2019, the Company borrowed from its CEO, $7,000
under a non-interest bearing promissory note which matures on
November 14, 2020 and was extended to December 31, 2020.
On March 1, 2020, the Company entered into a promissory notes
totaling $194,500 for the above notes, as an incentive to its CEO
for entering into this agreement, issued option to purchase 389,000
restricted common shares of the Company at $0.25 per share. The
option will be fully vested as of March 1, 2020.
On August 26, 2019, the Company borrowed from its CEO, $100,000
under a non-interest bearing promissory note which matures on
December 26, 2019.
On December 3, 2019, the Company borrowed from its CEO, $3,000
under a non-interest bearing promissory note which matures on
December 3, 2020.
On December 6, 2019, the Company borrowed from its CEO, $30,000
under a non-interest bearing promissory note which matures on
December 6, 2020.
On December 30, 2019, the Company borrowed from its CEO, $25,000
under a non-interest bearing promissory note which matures on
December 30, 2020.
On January 3, 2020, the Company borrowed from its CEO, $95,000
under a non-interest bearing promissory note which matures on
January 3, 2021.
On January 5, 2020, the related party exercised his option and
converted his note of $100,000 into 1,000,000 shares at $0.10 per
share.
On March 31, 2020, the Company borrowed from its CEO, $6,000 under
a non-interest bearing promissory note which matures on December
31, 2020.
NOTE 4 – PROMISSORY NOTES
During the year ended December 31, 2016, the Company borrowed
$480,000 under 7.5% Convertible Promissory Note Agreements. The
Notes were due September 30, 2017 and bore interest at 7.5%. The
noteholders had agreed to extend the maturity to October 31, 2017.
The notes were convertible into common stock of the Company at
$0.50 per share in the event of a voluntary conversion on or before
an optional prepayment or the maturity date, or (1) the lower of
$0.50 or (2) a 20% discount to the effective price per share
offering price in the event of a mandatory conversion upon
consummation of a “Qualified Financing”, as defined. The Company
had pledged all assets as security for the notes. In the event of
default, the notes would bear interest at 12% per annum.
Based upon the Company’s funding of $542,260, a Qualified
Financing, a mandatory conversion of the $480,000 in principal of
Convertible Notes was triggered. The $480,000 in principal plus
accrued interest were converted into 960,000 common shares and
three-year Warrants to purchase 144,000 common shares at $1.25 per
share.
Also on December 31, 2018, the Company borrowed an additional
$15,000, with interest payable annually at 4%, maturing on December
31, 2019. This note was paid in full on January 7, 2020.
During January 2019, the Company borrowed $20,000 under a
non-interest bearing promissory note which matures on December 31,
2019, this amount was converted to 13,334 shares of common stock in
2020.
On March 11, 2019, the Company borrowed $25,000 under a promissory
note bearing an annual interest rate of 5% and which matures on
September 11, 2019. The loan includes a warrant to purchase 12,500
common shares at a strike price of $1.25 per share. The warrant
expires in 3 years. This note was paid in full on January 16,
2020.
On March 14, 2019, the Company borrowed $25,000 under a promissory
note bearing an annual interest rate of 5% and which matures on
September 14, 2019 and was extended until December 31, 2020. The
loan includes a warrant to purchase 12,500 common shares at a
strike price of $1.25 per share. The warrant expires in 3
years.
On March 29, 2019, the Company borrowed $25,000 under a promissory
note bearing an annual interest rate of 5% and which matures on
September 29, 2019. The loan includes a warrant to purchase 12,500
common shares at a strike price of $1.25 per share. The warrant
expires in 3 years. This note was paid in full on January 21,
2020.
NOTE 5– INCOME TAXES
The Company’s deferred tax assets at consist of net operating loss
carry forwards of $4,393,785 Using a new federal statutory tax rate
of 21%, the valuation allowance balance as of March 31, 2021 total
of $0. The increase in the valuation allowance balance for the
three months ended March 31, 2021 of $26,615 is entirely
attributable to the net operating loss.
Due to the uncertainty of their realization, no income tax benefits
have been recorded by the Company for these loss carry forwards as
valuation allowances have been established for any such benefits.
The increase in the valuation allowance was the result of increases
in the net operating losses discussed above. Therefore, the
Company’s provision for income taxes is $-0- for the three months
ended March 31, 2021 and 2020.
At March 31, 2021 and December 31, 2020, the Company had no
material unrecognized tax benefits and no adjustments to
liabilities or operations were required. The Company does not
expect that its unrecognized tax benefits will materially increase
within the next twelve months. The Company recognizes interest and
penalties related to uncertain tax positions in general and
administrative expense. At March 31, 2021 and December 31, 2020,
the Company has not recorded any provisions for accrued interest
and penalties related to uncertain tax positions.
The Company files U.S. federal and state income tax returns in
jurisdictions with varying statutes of limitations.
NOTE 6 – STOCKHOLDERS’ DEFICIT
The Company is authorized to issue up to 100,000,000 shares of
common stock, $0.0001 par value per share plus 5,000,000 shares of
preferred stock, par value $0.0001.
On February 23, 2018, the board of directors of AVRA authorized the
issuance of an aggregate of 218,000 shares of AVRA’s common stock
(the “Shares”) as follows:
|
● |
150,000 Shares at a value of $1.25 per Share, to
six consultants and service providers for services rendered through
December 31, 2017; |
|
● |
35,000 Shares, at a value of $1.25 per Share, to
Farhan Taghizadeh, M.D., AVRA’s Chief Medical Officer, for services
rendered during the period September 1, 2017 to December 31, 2017;
and |
|
● |
19,500 and 13,500 Shares, at a value of $2.00 per
Share, to Barry F. Cohen and A. Christian Schauer, our Chief
Executive Officer and its former Chief Financial Officer,
respectively, pursuant to Conversion Agreements with each of such
officers, under which they converted all December 31, 2017 accrued
but unpaid compensation due them under their respective employment
agreements with the Company into the Shares. |
On August 13, 2018 the Company sold 16,000 shares of its common
stock for $20,000.
On October 4, 2018, the Board of Directors adopted the following
resolutions and took the following actions by unanimous written
consent in lieu of a meeting in accordance with the applicable
provisions of the Florida business Corporation Act:
|
● |
128,300 shares of restricted common stock
required to be issued, to six consultants and service providers for
services rendered through September 30, 2018; |
|
● |
400
shares of restricted common stock required to be issued, for
services rendered through February 28, 2018; |
On January 4, 2019, 115,050 Shares at a value of $1.25 per share
were issued for service rendered.
On April 1, 2019, 95,050 shares at a value ranging from $1.25-$2.41
per share were issued for services rendered.
On July 1, 2019, 79,672 shares at a value ranging from $1.25-$2.76
per share were issued for services rendered.
On August 28, 2019, 600,000 shares at a value ranging from
$1.25-$2.00 per share were issued for services rendered.
On December 1, 2019, the Company canceled 250,000 restricted shares
of the Company’s common stock that were previously issued under the
Stock Award letter dated August 28, 2019.
During the first quarter 2021, 1,025,000 shares at a value ranging
from $0.89-$1.07 per share were issued for services rendered.
Holders are entitled to one vote for each share of common stock. No
preferred stock has been issued.
NOTE 7 – 2016 INCENTIVE STOCK PLAN
On August 1, 2016, the Company adopted the 2016 Incentive Stock
Plan (the “Plan”). The Plan provides for the granting of options to
employees, directors, consultants and advisors to purchase up to
3,000,000 shares of the Company’s common stock. The Board is
responsible for administration of the Plan. The Board determines
the term of each option, the option exercise price, the number of
shares for which each option is granted and the rate at which each
option is exercisable. Incentive stock options may be granted to
any officer or employee at an exercise price per share of not less
than the fair market value per common share on the date of the
grant. On August 1, 2019, the Board increased the plan to
10,000,000 shares of common stock.
For options granted October 1, 2017, the following factors were
used: volatility 45.07%; expected term of 3 years, risk-free
interest rate of 2.00%, dividend yield of 0% and exercise price of
$1.25 per share.
For options granted July 1, 2018, the following factors were used:
volatility 31.34%; expected term of 3 years, risk-free interest
rate of 2.00%, dividend yield of 0% and exercise price of $1.25 per
share.
For options granted May 1, 2018, the following factors were used:
volatility 62.16%; expected term of 3 years, risk-free interest
rate of 2.00%, dividend yield of 0% and exercise price of $1.25 per
share.
On July 1, 2018 options for 75,000 shares were issued to our
Counsel for services rendered totaling $21,000. These shares are
vested immediately and expire on July 1, 2023. The exercise price
is $1.25.
For the year ended December 31, 2019 and 2018, 210,000 and -0-
options were exercised, respectively. Non-vested Options for 97,639
shares were forfeited during March 2018.
On December 1, 2019, the Company granted to its majority
shareholder options to purchase 750,000 common shares of the
Company at an exercise price per share will be $1.00. All shares
will immediately vest, and the Option will expire five years from
the date of issuance.
At December 31, 2019 and 2018 options representing 3,486,667 shares
and 2,243,250 shares were vested or exercisable, respectively.
All options issued to-date expire after five years from the issue
date. Except for the option for 1,750,000 shares issued to the CEO
and to the Company’s counsel for 40,000 shares that vested
immediately, all the options issued to date vest over three
years.
Stock options are accounted for in accordance with FASB ASC Topic
718, Compensation –Stock Compensation, with option expense
amortized over the vesting period based on the Black-Scholes
option-pricing model fair value on the grant date, which includes a
number of estimates that affect the amount of expense. During the
three months ended March 31, 2021 and 2020, $37,674 and $126,059
respectively, of expensed stock options has been recorded as
stock-based compensation and classified in general and
administrative expense on the Statement of Operations. The total
amount of unrecognized compensation cost related to non-vested
options was $217,229 as of March 31, 2021. This amount will be
recognized over a period of 42 months expiring September 30,
2024.
The grant date fair value of options granted during the year of
2018 and 2019 were estimated on the grant date using the
Black-Scholes model with the following assumptions:
For options granted May 1, 2018, the following factors were used;
volatility 62.16%; expected term of 3 years, risk-free interest
rate of 2.00%, dividend yield of 0% and exercise price of $1.25 per
share.
For options granted July 1, 2018, the following factors were used;
volatility 31.34%; expected term of 3 years, risk-free interest
rate of 2.00%, dividend yield of 0% and exercise price of $1.25 per
share.
For options granted February 1, 2019: Volatility 50.58%, term 3
years, risk-free interest rate of 2.00%, dividend yield of 0% and
exercise price of $2.00 per share. For options granted April 1,
2019: Volatility 48.52%, term 3 yrs, risk-free interest rate of
2.00%, dividend yield of 0% and exercise price of $1.25 per
share.
For options granted August 1, 2019: Volatility 62.43%, term 3
years, risk-free interest rate of 2.00%, dividend yield of 0% and
exercise price of $2.00 per share.
For options granted October 1, 2019: Volatility 48.57%, term 3
years, risk-free interest rate of 2.00%, dividend yield of 0% and
exercise price of $2.00 per share.
For options granted December 1, 2019: Volatility 61.91%, term 3
years, risk-free interest rate of 2.00%, dividend yield of 0% and
exercise price of $1.00 per share.
The grant date fair value of options granted during the year of
2020 were estimated on the grant date using the Black-Scholes model
with the following assumptions:
For options granted March 1, 2020 the fair market value is $0.45,
exercise $0.25, rate 2%, and volatility 39.73%.
No options were granted during the first three months of 2021
Option values are calculated using Black Scholes with the following
inputs: expected volatilities are based on the average volatilities
of six similar companies; fair market values are calculated using
the implied share values of recent company financings or OTC
closing prices for that day, whichever is more suitable; risk-free
rate used was 2%.
NOTE 8 – COMMITMENTS
Intellectual
property
Effective May 1, 2016, the Company entered into a Research
Agreement (the “Research Agreement”) with the University of Central
Florida (“UCF” or the “University”) for the development of a
prototype surgical robotic device supporting minimal invasive
surgical facial corrections.
The Agreement provides that the University will provide personnel
to accomplish the objectives as stated in the Statement of Work
over a period extending to September 30, 2017. Effective May 1,
2016, the research agreement with the University of Central Florida
has been extended to April 30, 2021. No additional payments to the
University were required.
The Company agreed to extend funding of $163,307 from AVRA’s
existing funds.
In addition, AVRA has paid $43,548 for outright ownership of the
University’s Intellectual Property resulting from the
collaboration, which amount is shown as Intellectual Property.
Management has assessed the carrying value of the asset at December
31, 2019 and has recorded an impairment loss in the amount of
$43,548.
For the three and nine months ended, September 30, 2020 and 2019,
$-0- had been paid under the Agreement. The balance of the amount
owing to the University was fully paid on February 24, 2017 and
April 7, 2017. Additionally, a $68,952 matching funds grant from
the Florida High Tech Corridor Council (FHTCC) was approved on July
16, 2016 which will provide the University research funds in
addition to the Company’s funding obligation to the University. The
FHTCC research grant is subject to certain research obligations and
action requirements which if not met may result in the loss of the
FHTCC research funding. The agreement further provides for the
payment of a 1% royalty to the University in any year when the
sales of products using the intellectual property exceeds
$20,000,000.
Employment
Agreements
On July 1, 2016, the Company entered into an Employment Agreement
with its Chairman and Chief Executive Officer. The agreement
provides for an annual salary of $120,000 per year, increasing to
$180,000 per year beginning July 2017. Through December 2016, the
employee agreed to not receive the compensation in cash until the
Board of Directors deemed it prudent to pay some or all of his
salary. Further the Agreement provides that the employee will
receive a three-year option to purchase 1,000,000 shares of the
Company’s common stock at an exercise price of $0.10 per share, and
becoming fully vested on August 15, 2016.
On August 1, 2016, the Company entered into a one-year Employment
Agreement with its Chief Financial Officer. The agreement provides
for an annual salary of $108,000 per year. Through December 2016,
the employee agreed to not receive the compensation in cash until
the Board of Directors deemed it prudent to pay some or all of his
salary. Further the Agreement provides that the employee will
receive a three-year option to purchase 210,000 shares of the
Company’s common stock at an exercise price of $0.10 per share,
with 70,000 shares becoming fully vested upon each yearly
anniversary. The options are to be surrendered and cancelled if the
Agreement is terminated. The Agreement has expired but its
compensation terms continue in effect as long as the employee
remains employed by the Company.
On August 1, 2016, the Company entered into a three-year Employment
Agreement with its Vice President of Global Business Development.
The agreement provides for an annual salary of $96,000 per year,
increasing to $144,000 per year beginning July 2017. Through
December 2016, the employee agreed to not receive the compensation
in cash until the Board of Directors deemed it prudent to pay some
or all of his salary. Further the Agreement provides that the
employee will receive a three-year option to purchase 300,000
shares of the Company’s common stock at an exercise price of $0.10
per share, with 100,000 shares vested on each yearly
anniversary.
Further, on July 1, 2016, the Company entered into Indemnification
Agreements with the Chairman and Chief Executive Officer, and on
August 1, 2016 the Chief Financial Officer and the Vice-President
of Global Business Development providing for the Company to
indemnify the individuals for all expenses, judgments, etc.
incurred while serving in various capacities with the Company.
Commencing March 1, 2018, the Company entered into an employment
agreement with its new Chief Strategy Officer whereby compensation
will be determined upon sufficient funding of the Company. The
Company granted a 300,000 share stock award under its 2016
Incentive Stock Plan, which vests in five equal annual installments
of 60,000 shares each.
In addition, on May 1, 2018 options for 250,000 shares that vest
monthly over 3 years were also issued to our Chief Strategy
Officer. These options expire on May 1, 2023 and are exercisable at
$1.25.
Commencing January 1, 2019, the Company entered into a consulting
agreement with an IR/PR Company whereby compensation will be $1,500
per month for six months. During third quarter 2019, these services
stopped. On July 1, 2019, the Company issued 36,000 restricted
common shares as part of the compensation.
Effective July, 1, 2020, the Company entered into an employee
agreement with its Chairman and Chief Executive Officer, for a term
of 48 months. The employee’s base salary is $15,000 monthly,
beginning with the July 2020 payment, which rate shall be inclusive
of all claims by the employee for his services. However, employee
agrees to accrue his salary from the July 1, 2020 through and
including December 2020 and allows the Board of Directors to decide
on whether to convert any or all accrued salary into Company
restricted common shares. Beginning on the July 1, 2020, normal
direct business expenses will be covered, including business class
travel on flights over 5 hours. Employee will receive a $500 per
month vehicle expense stipend to help mitigate the costs of the
frequent travel required to visit the Orlando office and University
of Central Florida from the employee’s home. Employee will also be
granted an option pursuant to the Company’s Equity Incentive Plan
to purchase 1,000,000 restricted shares of the Company’s common
stock, with an exercise price of $0.25 per share, and a Start Date
of July 1, 2020. All 1,000,000 shares will be fully vested on July
1, 2020.
Lease
The Company occupies office and laboratory space in Orlando,
Florida under a lease agreement that expired on July 31, 2018.
Effective August 1, 2018 and expiring July 31, 2019, the Company
signed a new agreement, with monthly payments of $1,829.25 plus
applicable sales tax. Effective August 1, 2019, the Company signed
a year lease agreement, provides that the Company pay insurance,
maintenance and taxes with a monthly lease expense of $2,454.75
plus applicable sales tax. Effective January 15, 2020, the Company
amended its August 1, 2019 lease agreement reducing its monthly
lease payment to $2,223 plus applicable sales tax. the Company
signed a lease that was effective August 1, 2020 through July 31,
2021, which provides that the Company pay insurance, maintenance
and taxes with a monthly lease expense of $1,474.17 plus applicable
sales tax.
Effective January 1, 2021, the Company signed an amendment
which modified the August 1, 2020 agreement, increasing the monthly
lease expense to $1,964.74 plus applicable sales
tax.
Either party may cancel the agreement at any time with 30 days’
notice.
NOTE 9 – OTHER MATTERS
On January 30, 2020, the World Health Organization (“WHO”)
announced a global health emergency because of a new strain of
coronavirus originating in Wuhan, China (the “COVID-19 outbreak”)
and the risks to the international community as the virus spreads
globally beyond its point of origin. In March 2020, the WHO
classified the COVID-19 outbreak as a pandemic, based on the rapid
increase in exposure globally.
The full impact of the COVID-19 outbreak continues to evolve as of
the date of this report. As such, it is uncertain as to the full
magnitude that the pandemic will have on the Company’s financial
condition, liquidity, and future results of operations. Management
is actively monitoring the global situation on its financial
condition, liquidity, operations, suppliers, industry, and
workforce. Given the daily evolution of the COVID-19 outbreak and
the global responses to curb its spread, the Company is not able to
estimate the effects of the COVID-19 outbreak on its results of
operations, financial condition, or liquidity for fiscal year
2020.
On March 27, 2020, President Trump signed into law the “Coronavirus
Aid, Relief, and Economic Security (CARES) Act.” The CARES act
was enacted as a response to the COVID-19 outbreak discussed above
and is meant to provide companies with economic
relief. The CARES Act, among other things, includes
provisions relating to refundable payroll tax credits, deferment of
employer side social security payments, net operating loss
carryback periods, alternative minimum tax credit refunds,
modifications to the net interest deduction limitations, increased
limitations on qualified charitable contributions, and technical
corrections to tax depreciation methods for qualified improvement
property.
NOTE 10 – SUBSEQUENT EVENTS
The Company has evaluated subsequent events through the date that
the financial statements were issued and determined that there were
subsequent events requiring adjustments to or disclosure in the
financial statements.
In July, 2021 several holders of stock options elected to exercise
their stock options with a cashless exercise provision resulting in
the issuance of 629,375 shares of common stock.
On September 22, 2021, the Company’s CEO, converted a total of
$50,000 of notes payable into 384,615 shares of common stock and
converted $50,000 of accrued salary into 384,615 shares of common
stock.
On October 1, 2021, the Company’s CEO, converted a total of
$595,000 of accrued salary into 5,950,000 shares of common stock at
a price of $0.10 per share and agreed to receive 450,000 shares of
common stock for $45,000 of the remaining salary due for the three
months ending December 31, 2021at a price of $0.10 per share.
On October 1, 2021, a former employee now a consultant elected to
convert a total of $251,500 of accrued consulting fees into
2,515,000 shares of common stock at a price of $0.10 per share,
converted $161,500 of accrued salary into 1,615,000 shares of
common stock at a price of $0.10 per share. and $4,500 of expenses
into 45,000 shares of common stock at a price of $0.10 per
share.
Between October 5, 2021 and December 8, 2021 the Company sold a
total of 2,229,231 shares of common stock at prices ranging between
$0.13 and $0.52 per share. The Company received proceeds of
$315,200.
On October 1, 2021 the Company issued a total of 1,500,000 of stock
options to consultants with an exercise price of $0.25 per
option.
On October 1, 2021 the Company issued 50,000 of stock options to
each of its independent Directors with an exercise price of $0.25
per option.
On October 1, 2021 the Company issued 350,000 of stock options to
its Chief Medical Officer with an exercise price of $0.25 per
option.
On October 1, 2021 the Company issued a total of 390,000 of stock
options to Company’s CEO with an exercise price of $0.25 per option
for the extension of loans.
On October 1, 2021 the Company issued a total of 174,553 shares of
common stock to several consultants.
On October 1, 2021 the Company issued 25,000 shares of common stock
to its Chief Medical Officer.
On July 1, 2022 the Company paid $5,000 and issued to a consultant
an option for 2,520,000 common shares with an exercise price of
$0.10 per share as a performance bonus and for foregoing all
accrued and unpaid fees due for 2022 and for foregoing a portion of
the fees due for the remaining five months of calendar year 2022.
The option vested immediately.
On July 1, 2022 the Company issued to its CEO an option for
5,400,000 common shares with an exercise price of $0.10 per share
as a performance bonus and for foregoing all of his 2022 salary.
The option vested immediately.
On July 1, 2022 the Company issued to its Chief Medical Officer an
option for 500,000 common shares with an exercise price of $0.10
per share as a performance bonus. The option vested
immediately.
On July 1, 2022 the Company issued to its Chief Strategy Advisor an
option for 500,000 common shares with an exercise price of $0.10
per share as a performance bonus. The option vested
immediately.
On July 1, 2022 the Company issued 240,270 shares of common stock
as payment in full for the accrued but unpaid fees due to its
Counsel.
On July 1, 2022 the Company issued 27,250 shares of common stock to
its patent attorney per their fee agreement.
On July 1, 2022 the Company issued 160,000 shares of common stock
to its Chief Strategy Officer as required by his Stock Grant Award
dated April 15, 2019 and his Employment Agreement dated March 1,
2018.
On July 1, 2022 the Company issued 40,000 shares of common stock to
its Chief Medical Officer as required by his employment agreement
dated September 15, 2020
On July 1, 2022 the Company issued a total of 569,747 shares of
common stock to several consultants.
In July 2022, four investors exercised their put options obtained
from the Offering dated October 26, 2020, transferred their
Membership Units in Avra Air LLC back to AVRA and received 301,027
shares of the Company’s common stock in return.
On July 25, 2022 the Directors and Shareholders holding a majority
of the issued and outstanding common shares of the Company adopted,
by joint written consent, a resolution to increase the Company’s
common stock reserved for issuance under the Company’s 2016
Incentive Stock Plan to 20,000,000.
On August 5, 2022, AVRA entered into a non-binding letter of intent
with Dr. Sudhir Srivastava (“Dr. Sudhir”), Cardio Ventures
Pvt. Ltd., a Bahamian private limited company of which Dr. Sudhir
is the sole stockholder(“Cardio”), Otto Pvt, Ltd., a
Bahamian private limited company and direct subsidiary of Cardio
(“Otto”) and Sudhir Srivastava Innovations Pvt. Ltd., an
Indian private limited company and indirect subsidiary of Cardio
(“SSI,” and together with Cardio and Otto, the “SSI
Parties”) with respect to a business combination between AVRA
and the SSI Parties (the “Transaction”). SSI, based in
Haryana, India is engaged in the development, commercialization,
manufacturing and sale of medical and surgical robotic systems
utilizing patents, trademarks and other intellectual property held
by Dr. Sudhir (the “SSI Intellectual Property”).
If and when the transaction is consummated, the business of the SSI
Parties, including the SSI Intellectual Property will be owned by
AVRA. The shareholders of the SSI Parties will own 95% of the
common stock of post-transaction AVRA and the current shareholders
of AVRA will own 5% of the common stock of post-transaction AVRA.
In addition, there will be changes in composition of the board of
directors, implementation of corporate governance policies and
changes in management, all with a view to listing the common stock
of AVRA on the Nasdaq Stock Market, LLC or another National
Securities Exchange. In addition, AVRA will change its name to
“SS Innovations, Inc.”
Consummation of the Transaction is subject to, among other matters,
the negotiation and execution of definitive agreements and
documentation, containing, in addition to the above terms, terms
and conditions customary for agreements of this type and nature,
including, without limitation, representations, warranties, and
indemnities of the parties.
Consummation of the Transaction is also subject to completion of a
due diligence review by each party of the other, the results of
which shall be satisfactory to the reviewing parties in their sole
discretion.
Given the foregoing, there can be no assurance given that the
Company will be able to successfully complete the Transaction.
In connection with executing the letter of intent, we advanced the
SSI Parties, the amount of $990,000 (the “Interim
Financing”). The Interim Financing is evidenced by two notes,
one for $100,000 and one for $1,000,000. Both are one-year
Automatically Convertible Notes made in favor of the Company by
Cardio, Otto and Dr Sudhir, jointly and severally (the “Cardio
Notes”). Interest on the Cardio Notes shall accrue at the rate
of 7% per annum, payable together with the principal amount at
maturity. The Cardio Notes have an original issue discount of 10%.
If the Cardio Notes are not repaid in full on or at maturity, they
will automatically convert into a percentage equity interest in
Cardio determined by dividing the principal amount of and accrued
interest on the Cardio Notes divided by $100 million. The Cardio
Notes contains customary default provisions and other typical terms
and conditions.
We may make additional advances to the SSI Parties of up to an
aggregate principal amount of $5,000,000 of Interim Financing,
evidenced by additional Cardio Notes. These Cardio Notes will be
substantially similar in form and substance to the first Cardio
Notes, provided, however, that Cardio Notes issued in
excess of an aggregate principal amount of $2.000,000, will have an
original issue discount of 6% as opposed to 10%, and the valuation
for determining conversion will be $250 million as opposed to $100
million.
In order to fund the Interim Financing, the Company offered and
sold to two accredited investors, $1,000,000 and $100,000 one-year
convertible promissory notes (the “Convertible Notes”). The
Convertible Notes will have the same interest rate and payment
terms as the Cardio Notes and otherwise be substantially similar to
the Cardio Notes, provided, however, that the
Convertible Notes do not have an original issue discount. Further,
upon consummation of the Transaction (if and when it is
consummated) the Convertible Notes will automatically convert into
a number of AVRA Shares determined by dividing the principal amount
of the Convertible Notes by $100 million and multiplying such
number expressed as a percentage by the number of AVRA Shares
issued to Dr. Sudhir and the other shareholders of the SSI Parties
(if any) upon closing of the Transaction. The Company may offer and
sell up to an aggregate principal amount of $5,000,000 in
Convertible Notes in order to fund the Interim Financing.
The Convertible Notes were issued in a private transaction pursuant
to the exemptions from registration under the Section 4(a)2 of the
Securities Act of 1933, as amended (the “Securities Act”)
and the rules and regulations promulgated thereunder.
In August 2022 the Company sold 1,000,000 shares of common stock at
a price of $0.25 per share receiving proceeds of $250,000.
In September 2022 and thru the date of this document, the Company
sold 1,631,000 shares of common stock at a price of $0.25 per share
receiving proceeds of $407,750.
Item 2. Management’s Discussion and Analysis of Financial
Condition and Results of Operations.
When used in this report, unless otherwise indicated, the terms
“Avra,” “the Company,” “we,” “us” and
“our” refer to Avra Medical Robotics, Inc.
Note Regarding Forward Looking Statements
This report contains forward-looking statements that reflect our
current views about future events. We use the words
“anticipate,” “assume,” “believe,”
“estimate,” “expect,” “will,” “intend,”
“may,” “plan,” “project,” “should,”
“could,” “seek,” “designed,”
“potential,” “forecast,” “target,”
“objective,” “goal” or the negatives of such terms or
other similar expressions. These statements relate to future events
or our future financial performance and involve known and unknown
risks, uncertainties and other factors that may cause our actual
results, levels of activity, performance or achievements to be
materially different from any future results, levels of activity,
performance or achievements expressed or implied by these
forward-looking statements.
Overview
We are a medical robotics company developing a fully autonomous
medical robotic system using proprietary software which integrates
Artificial Intelligence (“AI”) and Deep Learning, or machine
learning, (“DL”). By using an AI and DL enhanced software
program, we are creating an intelligent robotic system that we
believe can “robotize” a wide range of medical procedures
currently being performed by human hands. We are concentrating our
research and development efforts to meet rising expectations of
patients and practitioners alike for the precision, safety and
speed offered by an AI enhanced robotics platform system that can
be combined with proven medical devices, end-effectors and surgical
instruments.
We believe that progress in mechanical and software engineering has
made possible lightweight and relatively inexpensive robotic
devices for difficult procedures in various medical fields. Medical
robots are already being successfully employed in several areas of
surgery, including Urology (Prostate), Colo-Rectal, Gynecology,
Thoracic, General Surgery, Orthopedics, and Neuro and Spine
Surgery. Robots are also being used for Telemedicine and assistive
robotic methods are addressing the delivery of healthcare in
inaccessible locations, ranging from rural areas lacking specialist
expertise to post-disaster scenarios, and battlefield areas. With
the aging population dominating demographics in the U.S. across all
spectrums of healthcare, robotic technologies are being developed
toward promoting improved function, lower morbidity and improved
overall outcomes.
We are developing a treatment-independent autonomous robotics
system utilizing our proprietary AI-driven precision guidance
system, applicable to a variety of minimally and non-invasive
procedures, with an initial focus on skin resurfacing aesthetic
procedures utilizing several FDA approved skin enhancing techniques
robotized for superior performance and optimal results. Our medical
robotic system is being developed to deliver skin resurfacing
treatments, such as micro-needling and laser therapies with
improved efficiency, accuracy and precision over current procedures
conducted by human hand, and only requiring the doctor to input or
just confirm treatment parameters. As a result, use of our medical
robotic system is expected to provide improved quality and safety
as well as improve patient throughput and workflow.
Our autonomous medical robotics system is being developed to be
compatible with available FDA approved surgical tools and
end-effectors, enabling us to initially penetrate a sizable and
fast-growing aesthetics market, which includes micro-needling and
laser solutions. Our robotics system will allow doctors, and anyone
permitted to treat patients, defined at the State level, such as a
licensed aesthetician, to treat damaged skin autonomously by
delivering, for example, micro-needling to the skin. The
micro-needling catalyzes the natural process of collagen
remodeling, consisting of formation of new collagen, elastin, and
vascularization in the papillary dermis, similar to the effect of
laser treatments.
We expect our robotic system to eliminate many of the common errors
that occur during handheld procedures, such as over- or under-
exposure of the needles or energy-based instruments that can have
terrible cosmetic results and even injure the patient. In addition,
our system is being designed to continuously adjust treatment
parameters, such as penetration depth, time, and energy in order to
individualize the outcome based on our algorithms.
Our robotic system has been designed and developed through a
seamless collaboration of the surgeon, the engineer and the
scientist. Since the medical robotic industry has progressed
greatly in miniaturization, adaptability and lower costs, we
believe that the Avra “brains” technology component can lead
to dramatic opportunities in all of medicine.
The advantages of robotizing already FDA approved aesthetic devices
are many. In contrast to a human using a handheld device, our
aesthetics robotic system has the potential to perform each and
every procedure with unsurpassed precision without constraint of
age, proficiency, experience or fatigue. Likewise, in many skin
related treatments the amount of energy delivered, distance and/or
depth of the instrument to, or into, the skin, and treating only
the affected area are critical to the outcome. The robotic system
can maintain these parameters with unparalleled accuracy. The
system can also replicate the same procedure time and again
precisely. Delivery of certain aesthetic treatments by robotic
systems is believed to be the most efficient option, requiring
fewer visits per patient while increasing patient throughput — a
benefit for patients and practitioners alike.
Advantages of using our medical robotic approach to procedures
include:
|
● |
Reduced
cost per treatment. |
|
● |
Better
treatment accuracy. |
|
● |
Better
treatment outcomes. |
|
● |
Increased
patient throughput and revenue generation for the
physician. |
|
● |
Easier
multi-platform integration. |
|
● |
Addresses
shortfall of physicians/surgeons. |
|
● |
Easier
future integration of medical and technological advancements such
as molecular biologics. |
We believe that our initial medical robotic system for the
aesthetics market should find rapid acceptance based on the
aforementioned advantages of using the attribute of robotics versus
traditional manual applications. Furthermore, there is general
acceptance by consumers for fee-for-service cash payments in the
facial aesthetics market thereby avoiding medical insurance
reimbursement issues.
Our medical robotic system utilizes a robotic arm that has
7-degrees of freedom integrated with our proprietary AI-driven
control software and algorithms. The robotic arm was designed and
built under the required medical device standards of the U.S. Food
and Drug Administration (the “FDA”). Our strategy is to
integrate the robotic arm with FDA approved devices, which is
expected to allow for a more expedited approval of the integrated
system. We believe that the FDA approval process will primarily
focus upon validation of the medical robotic system’s software
control. This could lead to a less onerous, more de-risked
regulatory path to approval, particularly if strong preclinical
results are achieved. Subsequent to the completion of the FDA
preclinical work, estimated to take six months, we believe that we
will be able to additionally modify and robotize certain
non-invasive instruments that do not require FDA approvals and
proceed to the cosmetic treatments marketplace. This action could
sharply reduce the time to commercial operations and revenues.
We previously retained the services of The Horizon Phoenix Group
(“HPG”), a consulting firm experienced in securing U.S. and
foreign regulatory approvals for medical devices, in order to
initiate the regulatory process. Working with HPG, we prepared and
filed an application with the FDA for our initial medical robotic
system and in August 2019 held an initial pre-collaboration meeting
with the FDA. We believe that this is the first of a series of
meetings where the Avra system and its regulatory requirements will
be discussed in ever-increasing specificity. This should allow for
a more focused regulatory process, saving both resources and time.
The robotic arm that we intend to utilize for our system has
already been granted approval in the EU and received a CE mark. We
have begun implementing a quality and regulatory system that will
serve as the foundation for U.S., Canadian, European, Australian,
Japanese, and Brazilian market access for our medical robotic
system. The Medical Device Single Audit Program(“MDSAP”),
which we plan to employ, is a single inspection that, when
completed, is expected to support market access to these six most
important medical device marketplaces.
Since 2016, we had a research partnership with the University of
Central Florida (“UCF”) to develop a prototype intelligent
medical robotic system. UCF is recognized particularly for its work
in the area of medical robotic research and design, with a focus on
the guidance systems. Avra has paid UCF a one-time fee for outright
ownership of work developed by UCF in the collaboration. The
Research Agreement was extended several times and expired on April
30, 2021. To further the depth of our research and development we
also began a partnership in 2021 with Florida Polytechnic
University and are actively working with them on developing our
system. Avra recently brought in two Associate Professors and a
graduate to join Avra’s engineering development team. Effective
October 11th, 2021 Avra executed a Sponsored Student
Project Agreement which included two payments of $8,030 each
covering Fall semester in 2021 and Spring semester in 2022.
On September 10, 2019, we entered into a collaborative research and
development agreement with Infinite Mind, LLC, now known as Avra
Air, LLC (“Avra Air”). Avra Air is in the business of
developing computerized systems for robot operation and automation
employing software and AI for applications in various industries
and has more recently expanded to the development of air sanitizing
devices to help address such pathogens as COVID-19. Our CEO is also
an owner of Avra Air. Avra Air, with the use of Avra’s facilities
and cooperation of Avra personnel, will seek to develop software
and AI systems for robots that are relevant to the field of medical
treatment or diagnostics. As part of the collaboration, Avra Air
has granted Avra an exclusive, worldwide, full paid-up, perpetual,
royalty-free license to commercialize any technology (including any
patents) developed by Avra Air individually or jointly with Avra
during the term of the agreement as well as existing technology of
AVRA AIR in the field of medical robotics. This license survives
termination of the agreement.
On November 6, 2020, AVRA made an investment of $210,000 in Avra
Air which was made with $40,000 in cash and the balance by the
issuance to Avra Air of 472,222 restricted shares of our common
stock valued at $0.36 per share. In exchange for the investment.
Avra received (a) a 49.8% limited liability company membership
interest in Avra Air; and (b) the remaining 50% of a vehicular air
sterilization provisional patent that Avra did not yet control. In
addition, Avra also agreed to pay Avra Air a royalty payment of
$1.50 per vehicular air sterilization kit for two years from the
date that a first kit that uses the patent is sold. On December 22,
2020, the Company issued 472,222 shares of its common stock towards
the acquisition of its interest in Avra Air. Avra Air has recently
built a prototype portable air de-contaminant system which it plans
to market soon.
Our senior leadership team and advisory boards have broad and deep
experience in clinical practice, medical research, innovation and
development in the medical robotics field. We believe that our
team, which has been active in the medical robotics field for many
years, brings the necessary skills and experience to develop and
commercialize intelligent medical robotic systems, as well as in
marketing, supply chain management, and the implementation of all
other aspects of our planned business operations.
We believe we can rapidly develop and commercialize its initial
medical robotic system in the aesthetic skin resurfacing market
because of the following advantages and progress made to date,
including:
|
● |
Our
team is experienced in medical robotic engineering. |
|
● |
We
are working in conjunction with preeminent physicians, engineers
and scientific institutions. |
|
● |
We
have substantially completed the design phase and are ready to
complete a final, integrated prototype for the regulatory approval
process which has been initiated. |
|
● |
Our
robotic arm was built under the required medical device standards
of the FDA and has already received a CE Mark in
Europe. |
|
● |
Our
strategy is to integrate the robotic arm with FDA approved devices
for skin resurfacing, which we anticipate will allow for a more
expedited regulatory approval, with the FDA approval process
primarily focused upon validation of the medical robotic system’s
software control. We held a pre-collaboration meeting with the FDA
in August 2019, which should allow us to better focus on only the
meaningful required activities, saving both resources and
time. |
|
● |
We
have begun implementing a quality and regulatory system that will
serve as the foundation for U.S., Canadian, European, Australian,
Japanese, and Brazilian market access for AVRA’s medical robotic
system. MDSAP, which we plan to employ, is a single inspection
that, when completed, is expected to support market access to the
six most important medical device marketplaces. |
|
● |
We
believe that our treatment-independent medical robotics platform
system will be compatible with currently and yet to be approved
end-effectors and/or surgical tools enabling rapid entry into the
skin resurfacing and other markets with new and improved
devices. |
Results of Operations
Introduction
The financial statements appearing elsewhere in this report have
been prepared assuming the Company will continue as a going
concern. The Company was recently formed and has not established
sufficient operations or revenues to sustain the Company. These
conditions raise substantial doubt about the Company’s ability to
continue as a going concern.
The following table provides selected balance sheet data for our
Company at March 31, 2021 (unaudited) and December 31, 2020:
Balance Sheet
Data |
|
As
of |
|
|
As
of |
|
|
|
March 31, |
|
|
December 31, |
|
|
|
2021 |
|
|
2020 |
|
|
|
|
|
|
|
|
Cash |
|
$ |
316,813 |
|
|
$ |
160,709 |
|
Total Assets |
|
$ |
466,635 |
|
|
$ |
317,870 |
|
Total Liabilities |
|
$ |
1,226,140 |
|
|
$ |
1,186,919 |
|
Total Stockholders’ Deficit |
|
$ |
(759,504 |
) |
|
$ |
(869,049 |
) |
To date, the Company has relied on debt and equity raised in
private offerings and shareholder loans to finance operations and
no other sources of capital has been identified. If we experience a
shortfall in operating capital, we could be faced with having to
limit our research and development activities.
Three months ended March 31, 2021, as compared to three
months ended March 31, 2020
Revenues. We had no revenues during either the three months
ended March 31, 2021 or the three months ended March 31, 2020.
Research and Development Expenses. Research and development
expenses during the three months ended March 31, 2021 were $0, as
compared to $2,000 for the three months ended March 31, 2020.
Research and development expenses reflect continuing development
work on the Company’s prototype robotic system at its facilities at
UCF’s incubator in Orlando, Florida.
Compensation Expense. We had compensation expense of
$219,600 and $223,944 during the three months ended and no revenues
during either the three months ended March 31, 2021 and March 31,
2020, respectively. This includes compensation for the management
staff and stock-based compensation expense related to the Company’s
2016 Stock Incentive Plan.
General and Administrative Expenses. We incurred $80,477 and
$80,727 in general and administrative expenses during the three
months ended March 31, 2021 and March 31, 2020, respectively.
General and administrative expenses include legal and other
professional expenses related to the Company’s filings as a public
company with the Securities and Exchange Commission (the
“SEC”).
Other Income/Expenses. We had $22 interest earned in the
first three quarters of 2021 as compared to $344 of other expenses
during the three months ended March 31, 2020 consisting of interest
expense related to loans.
Net Loss. We incurred a net loss of $300,056 for the three
months ended March 31, 2021, as compared to a net loss of $307,015
for the three months ended March 31, 2020.
Liquidity and Capital Resources
The Company expects to require substantial funds for research and
development, to continue to develop, secure marketing approval for
and ultimately manufacture and market its initial medical robotic
system. Until the Company is able to generate revenues from the
sale of its initial medical robotic system, it expects to meet its
operating cash flow requirements from the net proceeds of this
Offering and if necessary, from future public or private sales of
its securities and, if possible, on favorable terms, by entering
into development partnerships to assist the Company with its
technology development activities.
During the period from inception (February 4, 2015) through March
21, 2020, the Company raised (a) $1,900 from an initial private
offering of its common stock in February 2017; (b) $480,000 from
the private offering of the convertible notes completed in June
2017; (c) $135,000 from a private offering of 135,000 shares of
common stock at a price of $1.00 per share completed in February
2017; (d) $542,260 from a private offering of 433,808 shares of
stock in a private offering at a price of $1.25 per share completed
in September 2017; and (e) $20,000 from the private sale of 16,000
shares of our common stock at a price of $1.25 per share in August
2018.
In March 2019, the Company sold 7.5 Units in a private offering of
ten (10) units (“Units”), each Unit consisting of a $10,000
principal amount six-month promissory note bearing interest at the
rate of 5% per annum and a three-year warrant to purchase 5,000
shares of common stock at an exercise price of $1.25 per share.
In addition to the foregoing, from December 2018 thru March 2020,
the Company obtained fourteen loans from Barry F. Cohen, our Chief
Executive Officer totaling $468,500. The loans were due 12 months
from funding date and did not bear interest. With the exception of
two loans totaling $145,000, all of these loans were subsequently
repaid in full via conversions into restricted company shares or
Units including one loan for $100,000 which was used to exercise a
stock option for 1,000,000 shares held by Mr. Cohen.
While we have been successful in raising funds to fund our
operations since inception and we believe that we will be
successful in obtaining the necessary financing to fund our
operations going forward, we do not have any committed sources of
funding and there are no assurances that we will be able to secure
additional funding. The accompanying financial statements have been
prepared assuming that the Company will continue as a going
concern; however, if the efforts noted above are not successful, it
would raise substantial doubt about the Company’s ability to
continue as a going concern. If we cannot obtain financing, then we
may be forced to further curtail our operations or consider other
strategic alternatives. Even if we are successful in raising the
additional financing, there is no assurance regarding the terms of
any additional investment and any such investment or other
strategic alternative would likely substantially dilute our current
shareholders.
Critical Accounting Policies
Use of Estimates
The preparation of financial statements in conformity with
accounting principles generally accepted in the United States
requires management to make estimates and assumptions that affect
the reported amounts of assets and liabilities and disclosures of
contingent assets and liabilities at the date of the financial
statements and the reported amounts of revenues and expenses during
the reporting period. Actual results could differ from
those estimates. Significant estimates included deferred
revenue, costs incurred related to deferred revenue, the useful
lives of property and equipment and the useful lives of intangible
assets.
Income Taxes
The Company accounts for income taxes in accordance with ASC 740,
Accounting for Income Taxes, as clarified by ASC 740-10, Accounting
for Uncertainty in Income Taxes. Under this method, deferred
income taxes are determined based on the estimated future tax
effects of differences between the financial statement and tax
basis of assets and liabilities given the provisions of enacted tax
laws. Deferred income tax provisions and benefits are
based on changes to the assets or liabilities from year to
year. In providing for deferred taxes, the Company
considers tax regulations of the jurisdictions in which the Company
operates, estimates of future taxable income, and available tax
planning strategies. If tax regulations, operating
results or the ability to implement tax-planning strategies vary,
adjustments to the carrying value of deferred tax assets and
liabilities may be required. Valuation allowances are
recorded related to deferred tax assets based on the “more likely
than not” criteria of ASC 740.
ASC 740-10 requires that the Company recognize the financial
statement benefit of a tax position only after determining that the
relevant tax authority would more likely than not sustain the
position following an audit. For tax positions meeting
the “more-likely-than-not” threshold, the amount recognized in the
financial statements is the largest benefit that has a greater than
50 percent likelihood of being realized upon ultimate
settlement with the relevant tax authority.
Off-Balance Sheet Arrangements
There are no off-balance sheet arrangements that have or are
reasonably likely to have a current or future effect on our
financial condition, changes in financial condition, revenues or
expenses, results of operations, liquidity, capital expenditures or
capital resources that is material to investors.
Item 3. Quantitative Disclosures About Market Risks.
As a “smaller reporting company,” we are not required to
provide the information required by this Item.
Item 4. Controls and Procedures.
Our Chief Executive Officer and Acting Chief Financial Officer, as
our principal executive, financial and accounting Officer,
conducted an evaluation of the effectiveness of the design and
operation of our disclosure controls and procedures, as defined in
Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of
1934, as amended (the “Exchange Act”), as of March 21, 2021,
to ensure that information required to be disclosed by us in the
reports filed or submitted by us under the Exchange Act is
recorded, processed, summarized and reported, within the time
periods specified in the rules and forms of the SEC, including to
ensure that information required to be disclosed by us in the
reports filed or submitted by us under the Exchange Act is
accumulated and communicated to our management, including our Chief
Executive Officer and Acting Chief Financial Officer, as our
principal executive, financial and accounting officer, or persons
performing similar functions, as appropriate to allow timely
decisions regarding required disclosure. Based on that evaluation,
our Chief Executive Officer and Acting Chief Financial Officer, as
our principal executive, financial and accounting officer, has
concluded that as of March 31, 2020, our disclosure controls and
procedures were not effective at the reasonable assurance level due
to the material weaknesses identified and described in Item 9A(b)
of our Annual Report on Form 10-K for the year ended December 31,
2019.
Our Chief Executive Officer and Acting Chief Financial Officer, as
our principal executive, financial and accounting officer, does not
expect that our disclosure controls or internal controls will
prevent all error and all fraud. Although our disclosure controls
and procedures were designed to provide reasonable assurance of
achieving their objectives and our principal executive officer has
determined that our disclosure controls and procedures are
effective at doing so, a control system, no matter how well
conceived and operated, can provide only reasonable, not absolute
assurance that the objectives of the system are met. Further, the
design of a control system must reflect the fact that there are
resource constraints, and the benefits of controls must be
considered relative to their costs. Because of the inherent
limitations in all control systems, no evaluation of controls can
provide absolute assurance that all control issues and instances of
fraud, if any, within the Company have been detected. These
inherent limitations include the realities that judgments in
decision-making can be faulty, and that breakdowns can occur
because of simple error or mistake. Additionally, controls can be
circumvented if there exists in an individual a desire to do so.
There can be no assurance that any design will succeed in achieving
its stated goals under all potential future conditions.
Changes in Internal Controls Over Financial Reporting
There were no changes in our internal controls over financial
reporting that occurred during the period covered by this report
that has materially affected, or is reasonably likely to materially
affect, our internal control over financial reporting.
PART II – OTHER
INFORMATION
Item 1. Legal Proceedings.
Not Applicable.
Item 1A. Risk Factors.
As a “smaller reporting company,” we are not required to
provide the information required by this Item.
Item 2. Unregistered Sales of Equity Securities and Use of
Proceeds.
During the first quarter of 2021, the Company issued 940,000,
shares without registration under the Securities Act of 1933, as
amended (the “Securities Act”). These shares were issued to
4 investors at a value of $0.25 per share.
These shares of our common stock were issued pursuant to the
exemptions from registration under the Securities Act afforded by
Section 4(a)(2) thereof and the rules and regulations
thereunder.
Item 3. Defaults Upon Senior Securities.
None.
Item 4. Mine Safety Disclosures.
Not applicable.
Item 5. Other Information.
None.
Item 6. Exhibits.
Exhibit No. |
|
Description
of Exhibit |
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31.1 |
|
Section
302 Certification |
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|
32.1 |
|
Section
906 Certification |
|
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|
101.INS |
|
Inline
XBRL Instance Document |
|
|
|
101.SCH |
|
Inline
XBRL Taxonomy Extension Schema Document |
|
|
|
101.CAL |
|
Inline
XBRL Taxonomy Extension Calculation Linkbase Document |
|
|
|
101.DEF |
|
Inline
XBRL Taxonomy Extension Definition Linkbase Document |
|
|
|
101.LAB |
|
Inline
XBRL Taxonomy Extension Label Linkbase Document |
|
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|
101.PRE |
|
Inline
XBRL Taxonomy Extension Presentation Linkbase Document |
|
|
|
104 |
|
Cover
Page Interactive Data File (formatted as Inline XBRL and contained
in Exhibit 101). |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of
1934, the registrant has duly caused this report to be signed on
its behalf by the undersigned thereunto duly authorized.
|
AVRA
MEDICAL ROBOTICS, INC. |
|
|
|
Dated:
November 3, 2022 |
By: |
/s/
Barry F. Cohen |
|
|
Barry
F. Cohen, Chief Executive Officer and
Acting Chief Financial Officer |
|
|
(Principal
Executive, Financial and
Accounting Officer) |
26
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