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Vitatronics

Country not established

Devices
1

What Vitatronics makes

Vitatronics makes the VITATRON 88 device.

The VITATRON 88 is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Vitatron 88 Ref K811939

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

Frequently asked questions

How many devices does Vitatronics have in the registry?

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

Which registries list Vitatronics's devices?

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

What risk classes do Vitatronics's devices fall under?

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

What are the newest devices from Vitatronics in the registry?

The most recently registered devices listed for Vitatronics include VITATRON 88.

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