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Envoy Medical Secures Three New Patents Strengthening Competitive Position in the Fully Implanted Hearing Space

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Envoy Medical (NASDAQ: COCH) announced issuance of three patents — one U.S. and two Hong Kong — strengthening its fully implanted cochlear implant IP portfolio.

The U.S. Patent No. 12,544,564 (Feb 10, 2026) covers improved input signal-to-noise ratio. Hong Kong patents HK40102155 and HK40107235 cover hearing-aid combination functionality and electrode impedance diagnostics. The company noted IP importance as it advances toward potential PMA submission; the Acclaim device holds FDA Breakthrough Device designation and is in a U.S. pivotal trial.

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Positive

  • U.S. Patent No. 12,544,564 granted Feb 10, 2026 for improved input signal-to-noise ratio
  • Two Hong Kong patents (HK40102155, HK40107235) expand system flexibility and diagnostics
  • FDA Breakthrough designation for Acclaim and ongoing U.S. pivotal trial

Negative

  • No PMA approved yet — regulatory approval and commercialization remain pending
  • Acclaim still investigational in a pivotal U.S. trial; commercialization timing is uncertain

Key Figures

New patents: 3 patents U.S. patent number: U.S. Patent No. 12,544,564 Hong Kong patent: HK40102155 +2 more
5 metrics
New patents 3 patents One U.S. patent and two Hong Kong patents for cochlear implant systems
U.S. patent number U.S. Patent No. 12,544,564 Granted February 10, 2026 for improved input signal-to-noise ratio
Hong Kong patent HK40102155 Combination hearing aid and cochlear implant system
Hong Kong patent HK40107235 Cochlear implant system with electrode impedance diagnostics
Breakthrough designation year 2019 FDA Breakthrough Device Designation for Acclaim cochlear implant

Market Reality Check

Price: $0.6960 Vol: Volume 397,216 is about 2...
low vol
$0.6960 Last Close
Volume Volume 397,216 is about 23% of the 1,726,948 20-day average, indicating muted trading interest pre-news. low
Technical Shares at 0.7102 are trading below the 200-day MA at 1.09, and are 62.82% under the 52-week high of 1.91 while still above the 0.3625 52-week low.

Peers on Argus

COCH was down 3.37% with light volume while sector peers showed mixed moves: RBO...
2 Up 2 Down

COCH was down 3.37% with light volume while sector peers showed mixed moves: RBOT up 8.41%, VVOS up 4.29%, IINN down 3.24%, TRIB down 3.06%. With 2 peers also moving down and a scanner summary citing broader dynamics (median move about -3.2% for decliners), part of COCH’s weakness pre-patent news aligned with sector forces rather than being purely idiosyncratic.

Historical Context

5 past events · Latest: Feb 19 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Feb 19 Clinical & financing update Positive -6.3% Upsized financing and pivotal trial progress with near-term enrollment completion.
Feb 17 Clinical trial update Positive +14.8% Nearing full enrollment and reiterating timeline to potential PMA submission.
Feb 12 Offering closing Negative -20.5% Closing of upsized public offering with significant new shares and warrants.
Feb 11 Offering pricing Negative +69.2% Pricing of large equity offering at $0.40 per share with attached warrants.
Dec 18 Enrollment milestone Positive -0.4% Pivotal Acclaim trial reached midway enrollment with timelines reaffirmed.
Pattern Detected

Recent history shows mixed reactions: positive clinical and financing news often met with selloffs, while one financing pricing event produced a strong rally. Overall, there are more divergence events than alignments between news tone and next-day price moves.

Recent Company History

Over the last few months, Envoy Medical has focused on funding and advancing its fully implanted Acclaim cochlear implant. In February 2026, it priced and then closed an upsized public offering linked to up to $78.0M, extending cash runway but prompting a sharp -20.52% reaction after closing. Clinical updates in December 2025 and mid‑February 2026 highlighted steady enrollment toward pivotal trial completion and a potential PMA submission in Q2 2027, yet some of these positive updates were followed by negative price moves. Against this backdrop, the new patent issuances add to a steadily building strategic IP and clinical story.

Market Pulse Summary

This announcement expands Envoy Medical’s intellectual property with three patents covering signal p...
Analysis

This announcement expands Envoy Medical’s intellectual property with three patents covering signal processing, integration with external hearing aids, and electrode impedance diagnostics for its fully implanted cochlear implant systems. These patents complement the Acclaim device’s existing FDA Breakthrough Device Designation from 2019 and its ongoing pivotal trial. Recent history shows frequent financings and mixed share-price reactions to otherwise positive updates, so investors may focus on how this strengthened patent estate supports future PMA submission, commercialization plans, and differentiation within hearing implants.

Key Terms

cochlear implant, signal-to-noise ratio, impedance diagnostics, compliance voltage, +3 more
7 terms
cochlear implant medical
"reinforcing its competitive position in the cochlear implant industry."
A cochlear implant is a surgically implanted medical device that converts sound into electrical signals and stimulates the inner ear to provide a sense of hearing for people with severe hearing loss, working like a tiny radio and wiring that bypasses damaged parts of the ear. Investors track cochlear implants because they involve durable hardware, ongoing service and upgrades, regulatory approvals, reimbursement rules and surgical volumes—factors that drive revenue, margins and long-term market growth.
signal-to-noise ratio technical
"titled "Cochlear Implant System with Improved Input Signal-to-Noise Ratio.""
The signal-to-noise ratio measures how much useful information (the signal) stands out from irrelevant or random data (the noise). For investors, a high ratio means price moves, earnings reports or research reliably reflect real value or trends, while a low ratio means it's harder to separate meaningful signals from meaningless fluctuations—like trying to hear a single voice in a crowded room or tune a radio to a clear station, which affects confidence in decisions.
impedance diagnostics medical
"Hong Kong Patent No. HK40107235, titled "Cochlear Implant System with Electrode Impedance Diagnostics,""
Impedance diagnostics measures how much a device or tissue resists electrical current, using simple electrical checks to spot changes, faults, or failures. For investors, it matters because these tests are used to verify the safety and performance of medical devices and monitoring systems—like using a car’s dashboard lights to flag problems—so reliable impedance data can influence regulatory approval, product recalls, maintenance costs, and market trust.
compliance voltage technical
"An example stimulation parameter can include a compliance voltage for the source element"
Compliance voltage is the maximum electrical pressure a medical device or regulated current source can produce while still delivering a steady, intended current; think of it as the highest water pressure a pump can use while keeping flow rate constant. For investors, it matters because it affects a device’s ability to reach and safely stimulate target tissue, influences battery life and component costs, and can be a factor in regulatory approval and market competitiveness.
Premarket Approval (PMA) regulatory
"progresses toward potential Premarket Approval (PMA) submission and commercialization"
Premarket Approval (PMA) is the strict regulatory review process used by the U.S. authority for high-risk medical devices to prove they are safe and effective before they can be sold. For investors, a granted PMA is like receiving a key to a locked market: it can open exclusive sales opportunities, reduce near-term competition, and justify higher valuations, while also signaling that the company has cleared a costly, time-consuming hurdle.
Breakthrough Device Designation regulatory
"The Acclaim4 cochlear implant received Breakthrough Device Designation from the FDA in 2019"
A breakthrough device designation is a regulatory program that gives promising medical devices for serious or life‑threatening conditions priority support and faster review from a health authority (e.g., the U.S. FDA). Think of it as a “fast lane” or VIP pass through development and review: it can shorten time to market, lower regulatory uncertainty, and boost a company’s commercial prospects — but it is not an approval by itself.
pivotal clinical trial medical
"and is currently under investigation as part of a U.S. based pivotal clinical trial."
A pivotal clinical trial is a late-stage medical study designed to provide the main evidence regulators use to decide whether a drug or medical device can be approved and sold; think of it as the product’s final exam. For investors, the trial’s outcome is critical because a clear pass can unlock regulatory approval, market access and future revenue, while failure can halt commercialization and materially affect a company’s valuation.

AI-generated analysis. Not financial advice.

White Bear Lake, Minnesota--(Newsfile Corp. - February 23, 2026) - Envoy Medical® Inc. (NASDAQ: COCH) ("Envoy Medical" or the "Company"), a hearing health company pioneering fully implanted hearing solutions, today announced the issuance of three new patents with one in the United States and two in Hong Kong, further expanding its intellectual property and reinforcing its competitive position in the cochlear implant industry.

"We believe the future of the cochlear implant industry is fully implanted devices and that our approach is novel when compared to other designs," said Brent Lucas, Chief Executive Officer of Envoy Medical. "As the industry realizes the wisdom and flexibility of our approach, we will have a strong patent portfolio to help protect our leadership position as a first mover with substantial differentiation."

Management believes that as the Company progresses toward potential Premarket Approval (PMA) submission and commercialization, the strength and breadth of its intellectual property portfolio will be an increasingly important asset, both strategically and competitively.

The United States Patent and Trademark Office granted U.S. Patent No. 12,544,564 on February 10, 2026, titled "Cochlear Implant System with Improved Input Signal-to-Noise Ratio." This patent relates to cochlear implant systems having a signal processor configured to filter a received input signal to attenuate a first pulse rate in the input signal and to output a stimulation signal based on the filtered input signal to cause a stimulator to provide electrical stimulation at the first pulse rate.

In addition, the Hong Kong Patent Office granted two complementary patents. Hong Kong Patent No. HK40102155, titled "Combination Hearing Aid and Cochlear Implant System." This patent relates to cochlear implant systems and receiving a status indicator signal indicative of whether an external auditory aid device (e.g., a hearing aid) is active and updating a transfer function of a signal processor of the cochlear implant system to compensate for operation of the external auditory aid device if it is active. This capability relates to the potential flexibility allowed by our system by leveraging the natural ear to pick up sound, which allows for (but does not require) the use of other devices in the ear.

Hong Kong Patent No. HK40107235, titled "Cochlear Implant System with Electrode Impedance Diagnostics," relates to impedance diagnostics within a cochlear implant system. This patent relates to impedance diagnostics in cochlear implant systems. A cochlear implant system can determine an impedance associated with a current path from a source element to a return electrode and determine one or more stimulation parameters for the source element based on the impedance. An example stimulation parameter can include a compliance voltage for the source element to provide a prescribed current.

The Acclaim® cochlear implant received Breakthrough Device Designation from the FDA in 2019 and is currently under investigation as part of a U.S. based pivotal clinical trial. For more information on the trial, visit www.envoymedical.com/acclaim-pivotal.

To be added to the Envoy Medical email distribution list, please email Envoy@kcsa.com with COCH in the subject line.

About Envoy Medical, Inc.
Envoy Medical (NASDAQ: COCH) is a hearing health company focused on providing innovative technologies across the hearing loss spectrum. Envoy Medical has pioneered one-of-a-kind, fully implanted devices for hearing loss, including its fully implanted Esteem® active middle ear implant, commercially available in the U.S. since 2010, and the fully implanted Acclaim® cochlear implant, an investigational device. Envoy Medical is dedicated to pushing hearing technology beyond the status quo to improve access, usability, compliance, and ultimately quality of life.

About the Fully Implanted Acclaim® Cochlear Implant
We believe the fully implanted Acclaim Cochlear Implant ("Acclaim CI") is a first-of-its-kind hearing device. 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.

CAUTION The fully implanted Acclaim Cochlear Implant is an investigational device. Limited by Federal (or United States) law to investigational use.

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.

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 operations; the ability to obtain additional patents and develop future products or product improvements; the ability to obtain and maintain compliance with Nasdaq rules and requirements; the timing and future outcome of its FDA pivotal trial; the ability to raise capital and the amount of capital required to complete the FDA pivotal trial and early commercialization; the Acclaim CI being the first to market fully implanted cochlear implant; the timing and results of activations, enrollments, follow-up visits, data, and clinical trials of the Acclaim CI; and the participation or any changes or delays in participation of any subjects, institutions, or healthcare professionals in such trials; the safety, performance, and market acceptance of the Acclaim CI; the timing and results of the Acclaim CI's PMA submission to the FDA; the size of Envoy Medical's addressable market, operational performance, future market conditions or economic performance and developments in the capital and credit markets; and 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; the ability to engage 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 March 31, 2025, 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.

Investor Contact:
Phil Carlson
KCSA Strategic Communications
O: 212.896.1233
E: Envoy@kcsa.com

Media Contact:
Anne Donohoe
KCSA Strategic Communications
O: 732-620-0033
E: Envoy@kcsa.com

To view the source version of this press release, please visit https://www.newsfilecorp.com/release/284835

FAQ

What patents did Envoy Medical (COCH) receive on February 23, 2026?

Envoy received three patents: one U.S. and two Hong Kong grants. According to the company, the U.S. patent is No. 12,544,564 and the Hong Kong patents are HK40102155 and HK40107235, covering signal processing, device combination, and impedance diagnostics.

How do Envoy Medical's new patents affect COCH shareholders?

The patents may strengthen Envoy's competitive IP position and protect differentiation. According to the company, the expanded portfolio is intended to support PMA progress and commercialization strategy, which could matter to investors assessing long-term value.

Does Envoy's U.S. patent No. 12,544,564 improve hearing performance?

The U.S. patent covers improved input signal-to-noise ratio in cochlear systems. According to the company, it describes filtering to attenuate a first pulse rate and output stimulation based on the filtered input to improve signal handling.

What do the Hong Kong patents HK40102155 and HK40107235 cover for COCH?

HK40102155 covers combination use with external hearing aids; HK40107235 covers electrode impedance diagnostics. According to the company, these patents enable device flexibility and parameter adjustments based on measured impedance.

What is the regulatory status of Envoy's Acclaim device (COCH)?

Acclaim has FDA Breakthrough Device designation but no PMA yet. According to the company, Acclaim is under investigation in a U.S. pivotal clinical trial as the company progresses toward potential PMA submission.
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