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Cleveland Clinic Foundation

Country not established

Devices
1

What Cleveland Clinic Foundation makes

The Cleveland Clinic Foundation makes the Vanguard System, a medical device used for specific clinical applications as indicated by its classification.

The Vanguard System is a Class II device listed in the FDA 510(k) registry, and the manufacturer is based in the United States.

AI-generated from registry data, 24 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • The Vanguard System Ref K941551

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

Frequently asked questions

How many devices does Cleveland Clinic Foundation have in the registry?

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

Which registries list Cleveland Clinic Foundation's devices?

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

What risk classes do Cleveland Clinic Foundation's devices fall under?

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

What are the newest devices from Cleveland Clinic Foundation in the registry?

The most recently registered devices listed for Cleveland Clinic Foundation include THE VANGUARD SYSTEM.

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