MEDTEOR GmbH
DE-MF-000019576 · Germany · Oppenau
MEDTEOR GmbH is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|---|
| Class IIb | 9 |
Most frequent device types declared: Scanbody, Screw, Screwdriver, Titan Base.
Among these devices, 9 are declared implantable, 4 reusable.
Catalogue references include D-MA35-C0G4-AS, D-MA35-C1G2-AS, D-MA35-C2G3-AS, D-MA35-C2G4-AS, MTO-D2T5-60, MTO-DIT5-10-BOX.
European nomenclature codes declared: P01020180.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 17 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. MEDTEOR GmbH was not found in either the U.S. or the Canadian register.