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Corvista Health, Inc.

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Devices
1

What Corvista Health, Inc. makes

Corvista Health, Inc. manufactures the CorVista® System, a medical device designed for diagnostic imaging of coronary arteries using intravascular ultrasound (IVUS) technology.

The CorVista® System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. 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

  • CorVista® System Ref K232686

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

Frequently asked questions

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

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

Which registries list Corvista Health, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Corvista Health, Inc. include CorVista® System.

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