SILADENT Dr. Böhme & Schöps GmbH
DE-MF-000052689 · Germany · Goslar
SILADENT Dr. Böhme & Schöps GmbH is registered in the European database on medical devices as a manufacturer, with 31 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 31 |
|---|
Most frequent device types declared: Alu-Bisswachs, Aufstellwachs, Biss-Stangen, Bisswälle, Set-Up Plattenwachs.
Devices declared under this manufacturer
- Alu-Bisswachs, grau, 175 x 80 x 2 mm, 250 g
- Aufstellwachs blau 3 x 3 mm, 220 g
- Aufstellwachs hellrosa 5 x 5 mm, 220 g
- Biss-Stangen hart gelb 50 Stück
- Biss-Stangen hart rot, 50 Stück - Sondermischung
- Biss-Stangen medium gelb, 50 Stück
- Bisswälle hart rot 100 Stück
- Bisswälle hart rot, 1 Stück - Muster
- Bisswälle medium rot 100 Stück
- Bisswälle soft rot
- Bisswälle soft rot 100 Stück
- Muster Set-Up Plattenwachs hard (Sommer), 1 Platte
Showing 12 of 31 declared devices.
Catalogue references include 02-4110, 02-4255, 02-4265, 02-4300, C02-4200, C02-4210.
European nomenclature codes declared: Q01020203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 31 |
| 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 | 31 |
|---|---|
| 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. SILADENT Dr. Böhme & Schöps GmbH was not found in either the U.S. or the Canadian register.