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FDA 510(k)

Lyric4 Hearing Aid

K-Number: K232999 · 2024-04-11

ApplicantSonova AG
Decision Date2024-04-11
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Lyric4 Hearing Aid is the device name listed in this FDA 510(k) record. The listed applicant is Sonova AG. It received FDA 510(k) clearance on 2024-04-11 under 510(k) number K232999. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lyric4 Hearing Aid?

Lyric4 Hearing Aid is a medical device that received FDA 510(k) clearance on 2024-04-11. The listed applicant is Sonova AG. The 510(k) number is K232999.

When did Lyric4 Hearing Aid receive FDA 510(k) clearance?

Lyric4 Hearing Aid received FDA 510(k) clearance on 2024-04-11, under 510(k) number K232999.

Who is the listed applicant for Lyric4 Hearing Aid?

The FDA 510(k) record lists Sonova AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Lyric4 Hearing Aid?

The FDA product code for Lyric4 Hearing Aid is ESD.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT06138665Evaluation of a New Noise Reduction Strategy in Hearing AidsCOMPLETEDNCT07501312Remote Microphone Performance Comparison in Adults With Hearing LossCOMPLETEDNCT07711249Clinical Benefit of Hearing Aid Tinnitus Feature on Tinnitus-Related Annoyance in Tinnitus Patients in BelgiumNOT_YET_RECRUITINGNCT07224919AutoFocus360 Sound Quality Preference and Claims StudyCOMPLETEDNCT07414329Efficacy and Effectiveness of an Investigational Behind-the-Ear Hearing Device KitCOMPLETEDNCT07526428Investigating the DNN Noise Reduction Feature in Phonak Hearing Aids Using Ecological Momentary AssessmentTERMINATED

Other records listing Sonova AG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K230538All-Day Clear Slim ADCS1 Hearing Aid. All-Day Clear ADC1 Hearing Aid

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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