Müller-Omicron GmbH & Co.KG
DE-MF-000012806 · Germany · Lindlar
Müller-Omicron GmbH & Co.KG is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 15 |
|---|
Most frequent device types declared: A-silicones, bite registration materials.
Devices declared under this manufacturer
- PLU°LINE A-SILIKON HEAVY BODY 5:1
- PLU°LINE A-SILIKON LIGHT BODY
- PLU°LINE A-SILIKON LIGHT BODY FAST
- PLU°LINE A-SILIKON MEDIUM BODY
- PLU°LINE A-SILIKON PUTTY
- PLU°LINE A-SILIKON PUTTY SOFT
- PLU°LINE A-SILIKON PUTTY SOFT 5:1
- SIMPLEE® Silic A Light
- SIMPLEE® Silic A Light fast
- SIMPLEE® Silic A Medium
- SIMPLEE® Silic A Putty
- SIMPLEE® Silic A Putty soft
Showing 12 of 15 declared devices.
Catalogue references include 000082505, 000085129, 002285121, 002285123, 002288900, 008082501.
European nomenclature codes declared: Q01020104.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| 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. Müller-Omicron GmbH & Co.KG was not found in either the U.S. or the Canadian register.