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FDA PMA

Implant, hearing, active, middle ear, totally implanted

Número do PMA: P090018 · 2026-06-03

RequerenteEnvoy Medical Corporation
Data da decisão2026-06-03
Número PMAP090018
Código do produtoOAF
Classe do DispositivoClasse 3
Especialidade MédicaU
Comité consultivoEN

Resumo do dispositivo

Implant, hearing, active, middle ear, totally implanted is the device name listed in this FDA 510(k) record. The listed applicant is Envoy Medical Corporation. It received FDA 510(k) clearance on 2026-06-03. The device is classified under product code OAF. It was reviewed by the EN advisory panel.

Perguntas frequentes

What is the Implant, hearing, active, middle ear, totally implanted?

Implant, hearing, active, middle ear, totally implanted is a medical device that received FDA 510(k) clearance on 2026-06-03. The listed applicant is Envoy Medical Corporation.

When did Implant, hearing, active, middle ear, totally implanted receive FDA 510(k) clearance?

The clearance date for Implant, hearing, active, middle ear, totally implanted can be found in the official FDA records.

Who is the listed applicant for Implant, hearing, active, middle ear, totally implanted?

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

What is the FDA product code for Implant, hearing, active, middle ear, totally implanted?

The FDA product code for Implant, hearing, active, middle ear, totally implanted is OAF.

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Fonte oficial

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