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Ear Masters, Inc.

Country not established

Devices
1

What Ear Masters, Inc. makes

Ear Masters, Inc. makes hearing aids, specifically all-in-the-ear hearing aids.

The company's devices are classified as Class I medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 21 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Hearing Aid (All-In-The-Ear) Ref K924350

    Active Regimes: 510(k) Registry: 510(k) Class:I

Frequently asked questions

How many devices does Ear Masters, Inc. have in the registry?

The registry currently lists 1 device for Ear Masters, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ear Masters, Inc.'s devices?

Among its 1 most recently registered device, Ear Masters, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Ear Masters, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Ear Masters, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Ear Masters, Inc. in the registry?

The most recently registered devices listed for Ear Masters, Inc. include HEARING AID (ALL-IN-THE-EAR).

Generated automatically from registry data and not verified by a human reviewer.