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KINVENT Biomecanique

FR-MF-000031884 · France · Montpellier

KINVENT Biomecanique is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa12

Among these devices, 11 are declared active.

No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.

United States market access

FDA establishment registerRegistered with FDA
Matched entryKINVENT BIOMECANIQUE (FR) · FDA 3016566173
Devices in EUDAMED12
Country of registrationFrance

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