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Audimax

Country not established

Devices
1

What Audimax makes

Audimax manufactures the Audiometer Model-500, a diagnostic device used to measure hearing sensitivity and assess auditory function in clinical settings.

The Audiometer Model-500 is classified as a Class II medical device and is listed under FDA’s 510(k) clearance process. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Audiometer Model-500 Ref K831431

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Audimax have in the registry?

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

Which registries list Audimax's devices?

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

What risk classes do Audimax's devices fall under?

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

What are the newest devices from Audimax in the registry?

The most recently registered devices listed for Audimax include AUDIOMETER MODEL-500.

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