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Vital 5

Country not established

Devices
1

What Vital 5 makes

Vital 5 manufactures the VITAL 5 RELEAF CATHETER, a medical device designed for specific therapeutic purposes.

The company is based in the US, and its catheter is classified as a Class II device, listed in the FDA 510(k) registry.

AI-generated from registry data, 27 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Vital 5 Releaf Catheter Ref K122661

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

Frequently asked questions

How many devices does Vital 5 have in the registry?

The registry currently lists 1 device for Vital 5. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vital 5's devices?

Among its 1 most recently registered device, Vital 5 has devices listed in FDA 510(k) (1 device).

What risk classes do Vital 5's devices fall under?

Among its 1 most recently registered device, the classes recorded for Vital 5's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Vital 5 in the registry?

The most recently registered devices listed for Vital 5 include VITAL 5 RELEAF CATHETER.

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