Skip to content

Zenith/Omni Hearing Instruments, Inc.

Country not established

Devices
1

What Zenith/Omni Hearing Instruments, Inc. makes

Zenith/Omni Hearing Instruments, Inc. manufactures in-the-ear hearing aids.

These 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, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • In The Ear Hearing Aid Ref K915450

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does Zenith/Omni Hearing Instruments, Inc. have in the registry?

The registry currently lists 1 device for Zenith/Omni Hearing Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Zenith/Omni Hearing Instruments, Inc.'s devices?

Among its 1 most recently registered device, Zenith/Omni Hearing Instruments, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Zenith/Omni Hearing Instruments, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Zenith/Omni Hearing Instruments, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Zenith/Omni Hearing Instruments, Inc. in the registry?

The most recently registered devices listed for Zenith/Omni Hearing Instruments, Inc. include IN THE EAR HEARING AID.

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