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Yperion Technology

FranceFDA applicant, unverified

Devices
1

What Yperion Technology makes

Yperion Technology manufactures the OR-LIGHT, a surgical lighting device designed for operating rooms to provide high-intensity illumination for precise medical procedures.

The OR-LIGHT is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. 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

  • Or-Light Ref K090724

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

Frequently asked questions

How many devices does Yperion Technology have in the registry?

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

Which registries list Yperion Technology's devices?

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

What risk classes do Yperion Technology's devices fall under?

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

What are the newest devices from Yperion Technology in the registry?

The most recently registered devices listed for Yperion Technology include OR-LIGHT.

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