EU → North America Device Access

Thanner GmbH

DE-MF-000032767 · Germany · Höchstädt

Thanner GmbH is registered in the European database on medical devices as a manufacturer, with 908 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa908

Most frequent device types declared: Achillessehnen-Entlastungsschuhe, CuraPro Verbandschuhe Langzeit, CuraPro Vorfußentlastungsschuhe, Diabeticus+Rheumaticus, Diabeticus+Rheumaticus® Socken für Diabetiker.

Devices declared under this manufacturer

Showing 12 of 908 declared devices.

Catalogue references include 4.1160, 4.4645, 4.5174, 4.5176, 5.3031, 5.3320.

European nomenclature codes declared: Y063303, Y090327, Y06120601, Y061203, Y06121201.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED908
Country of registrationGermany

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Devices with a numeric GTIN908
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. Thanner GmbH was not found in either the U.S. or the Canadian register.

Other manufacturers in Germany

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