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Gmv Aerospace and Defence S.A.

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Devices
1

What Gmv Aerospace and Defence S.A. makes

Gmv Aerospace and Defence S.A. manufactures the RADIANCE system, a medical device designed for imaging and diagnostic purposes in aerospace and defense applications, supporting real-time monitoring and analysis of physiological data.

The RADIANCE 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

  • Radiance Ref K112060

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

Frequently asked questions

How many devices does Gmv Aerospace and Defence S.A. have in the registry?

The registry currently lists 1 device for Gmv Aerospace and Defence S.A.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Gmv Aerospace and Defence S.A.'s devices?

Among its 1 most recently registered device, Gmv Aerospace and Defence S.A. has devices listed in FDA 510(k) (1 device).

What risk classes do Gmv Aerospace and Defence S.A.'s devices fall under?

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

What are the newest devices from Gmv Aerospace and Defence S.A. in the registry?

The most recently registered devices listed for Gmv Aerospace and Defence S.A. include RADIANCE.

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