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Cami, Inc.

Country not established

Devices
1

What Cami, Inc. makes

Cami, Inc. manufactures the AUDTEX 85, a device designed for audiometric testing to measure hearing thresholds in clinical settings.

The AUDTEX 85 is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Audtex 85 Ref K853895

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

Frequently asked questions

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

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

Which registries list Cami, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Cami, Inc. include AUDTEX 85.

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