Kettenbach-Dental GmbH
DE-MF-000053527 · Germany · Eschenburg
Kettenbach-Dental 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 | 17 |
|---|
Among these devices, 7 are declared implantable.
Devices declared under this manufacturer
- Visalys BioCeramic Block Chroma A0
- Visalys BioCeramic Block Chroma A2
- Visalys BioCeramic Block Chroma A3
- Visalys BioCeramic Block Implant Chroma A0 øL
- Visalys BioCeramic Block Implant Chroma A1 øS
- Visalys BioCeramic Block Implant Chroma A2 øL
- Visalys BioCeramic Block Implant Chroma A2 øS
- Visalys BioCeramic Block Implant Chroma A3 øL
- Visalys BioCeramic Block Implant Chroma A3 øS
- Visalys BioCeramic Block Implant Translucent øL
- Visalys BioCeramic Block Implant Translucent øS
- Visalys BioCeramic Block Intro pack
Showing 12 of 17 declared devices.
Catalogue references include 1507199, 1507499, 1507599, 1507699, 1508399, 1508499.
European nomenclature codes declared: Q010699.
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.
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. Kettenbach-Dental GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
20647GB448260629 | issued | 2031-06-26 |