EU → US Device Access

Ritter Implants GmbH & Co. KG

DE-MF-000006414 · Germany · Biberach

Ritter Implants GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 895 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa895

Most frequent device types declared: Dental Tools, Temporary Abutments, Surgical Kits, Dental Drills and Surgical Kits, Laboratory Analogs.

Among these devices, 3 are declared sterile, 111 reusable, 213 with a measuring function.

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 entryRitter Implants GmbH & Co. KG (DE) · FDA 3009528809
Devices in EUDAMED895
Country of registrationGermany

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