Envoy Medical Awarded Patent for Recharge System used with Implantable Battery
September 16 2024 - 9:00AM
Envoy Medical®, Inc. (“Envoy Medical”) (NASDAQ: “COCH”), a hearing
health company focused on fully implanted hearing systems, today
announces it has been awarded another patent from the US Patent
& Trademark Office for its fully implanted devices. On
September 3rd, the Company was issued Patent No. 12,081,061,
“Recharge System for Implantable Battery,” which relates to
predicting a cumulative thermal dose associated with charging an
implantable rechargeable energy storage device to a fully charged
state and adjusting the amount of current provided to the device
during charging. In other words, this can be used to maintain a
safe temperature of an implanted rechargeable battery during
recharging.
“We are pleased to continue to add to our growing portfolio of
patents as we further develop our innovative technologies,” said
Envoy Medical CEO Brent Lucas. “Maintaining safe battery
temperatures during recharging is an important risk mitigation for
any implanted medical device, and we believe we have patented an
effective solution for our products.”
About the Esteem® Fully Implanted Active Middle Ear
Implant (FI-AMEI)
The Esteem fully implanted active middle ear implant (FI-AMEI)
is the only FDA-approved, fully implanted* hearing device for
adults diagnosed with moderate to severe sensorineural hearing loss
allowing for 24/7 hearing capability using the ear’s natural
anatomy. The Esteem FI-AMEI hearing implant is invisible and
requires no externally worn components and nothing is placed in the
ear canal for it to function. Unlike hearing aids, you never put it
on or take it off. You can’t lose it. You don’t clean it. The
Esteem FI-AMEI hearing implant offers true 24/7 hearing.
*Once activated, the external Esteem FI-AMEI Personal Programmer
is not required for daily use.
Important safety information for the Esteem FI-AMEI can be found
at: https://www.envoymedical.com/safety-information.
About the Fully Implanted Acclaim® Cochlear
Implant
We believe the fully implanted Acclaim Cochlear Implant
(“Acclaim CI”) will be a first-of-its-kind fully implanted cochlear
implant. Envoy Medical’s fully implanted technology includes a
sensor designed to leverage the natural anatomy of the ear instead
of a microphone to capture sound.
The Acclaim CI is designed to address severe to profound
sensorineural hearing loss that is not adequately addressed by
hearing aids. The Acclaim CI is expected to be indicated for adults
who have been deemed adequate candidates by a qualified
physician.
The Acclaim Cochlear Implant received the Breakthrough Device
Designation from the U.S. Food and Drug Administration (FDA) in
2019. We believe the Acclaim CI was the first hearing-focused
device to receive Breakthrough Device Designation.
CAUTION The fully implanted Acclaim Cochlear Implant is
an investigational device. Limited by Federal (or United States)
law to investigational use.
Additional Information and Where to Find It
Copies of the documents filed by Envoy Medical with the SEC may
be obtained free of charge at the SEC’s website at www.sec.gov.
Forward-Looking Statements
This press release includes “forward-looking statements” within
the meaning of the “safe harbor” provisions of the United States
Private Securities Litigation Reform Act of 1995. Forward-Looking
statements may be identified by the use of words such as
“estimate,” “plan,” “project,” “forecast,” “intend,” “will,”
“expect,” “anticipate,” “believe,” “seek,” “target” or other
similar expressions that predict or indicate future events or
trends or that are not statements of historical matters, but the
absence of these words does not mean that a statement is not
forward-looking. Such statements may include, but are not limited
to, statements regarding the expectations of Envoy Medical
concerning the outlook for its business, productivity, plans and
goals for future operational improvements and capital investments;
the benefits of intellectual property developed by Envoy; the
potential for passage of legislation related to reimbursement for
active middle ear hearing devices; the impact that such proposed
legislation might have on the hearing health market, reimbursement
for the Esteem FI-AMEI device, and the Envoy Medical business, and
future market conditions or economic performance, as well as any
information concerning possible or assumed future operations of
Envoy Medical. The forward-looking statements contained in this
press release reflect Envoy Medical’s current views about future
events and are subject to numerous known and unknown risks,
uncertainties, assumptions and changes in circumstances that may
cause its actual results to differ significantly from those
expressed in any forward-looking statement. Envoy Medical does not
guarantee that the events described will happen as described (or
that they will happen at all). These forward-looking statements are
subject to a number of risks and uncertainties, including, but not
limited to changes in the market price of shares of Envoy Medical’s
Class A Common Stock; changes in or removal of Envoy Medical’s
shares inclusion in any index; Envoy Medical’s success in retaining
or recruiting, or changes required in, its officers, key employees
or directors; unpredictability in the medical device industry, the
regulatory process to approve medical devices, and the clinical
development process of Envoy Medical products; competition in the
medical device industry, and the failure to introduce new products
and services in a timely manner or at competitive prices to compete
successfully against competitors; disruptions in relationships with
Envoy Medical’s suppliers, or disruptions in Envoy Medical’s own
production capabilities for some of the key components and
materials of its products; changes in the need for capital and the
availability of financing and capital to fund these needs; changes
in interest rates or rates of inflation; legal, regulatory and
other proceedings could be costly and time-consuming to defend;
changes in applicable laws or regulations, or the application
thereof on Envoy Medical; a loss of any of Envoy Medical’s key
intellectual property rights or failure to adequately protect
intellectual property rights; the effects of catastrophic events,
including war, terrorism and other international conflicts; and
other risks and uncertainties set forth in the section entitled
“Risk Factors” and “Cautionary Note Regarding Forward Looking
Statements” in the Annual Report on Form 10-K filed by Envoy
Medical on April 1, 2024, and in other reports Envoy Medical files,
with the SEC. If any of these risks materialize or Envoy Medical’s
assumptions prove incorrect, actual results could differ materially
from the results implied by these forward-looking statements. While
forward-looking statements reflect Envoy Medical’s good faith
beliefs, they are not guarantees of future performance. Envoy
Medical disclaims any obligation to publicly update or revise any
forward-looking statement to reflect changes in underlying
assumptions or factors, new information, data or methods, future
events or other changes after the date of this press release,
except as required by applicable law. You should not place undue
reliance on any forward-looking statements, which are based only on
information currently available to Envoy Medical.
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Investor Contact:CORE
IR516-222-2560investorrelations@envoymedical.com
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