WIELAND Edelmetalle GmbH
DE-MF-000006997 · Germany · Pforzheim
WIELAND Edelmetalle GmbH is registered in the European database on medical devices as a manufacturer, with 144 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 144 |
|---|
Among these devices, 144 are declared implantable.
Devices declared under this manufacturer
- CoCrMo6 Fraesrohling 98,5x12mm mit Nut
- CoCrMo6 Fraesrohling 98,5x13,5mm
- CoCrMo6 Fraesrohling 98,5x16mm
- DENTONEM 98x10mm
- DENTONEM 98x13,5mm
- DENTONEM 98x20mm
- Disque de chrome cobalt 18 mm
- Disque de chrome cobalt 20 mm
- GQ Quattro Disc NEM Soft 12 mm Ø 98,5 mit Nut
- GQ Quattro Disc NEM Soft 8 mm Ø 98,5
- Galvano NEO
- NEM/CoCr Blank
Showing 12 of 144 declared devices.
Catalogue references include 22.000.C13, 22.000.C20, 2570200160, 2570300180, 2570300200, 30909820.
European nomenclature codes declared: Q010601.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 144 |
| 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 | 144 |
|---|---|
| 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. WIELAND Edelmetalle GmbH was not found in either the U.S. or the Canadian register.