EU → US Device Access

Laboratoires Anios

FR-MF-000011756 · France · Lezennes

Laboratoires Anios is registered in the European database on medical devices as a manufacturer, with 277 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa237
Class IIb40

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 registerNot found in the FDA register
Devices in EUDAMED277
Country of registrationFrance
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.

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