Dr. Hinz Dental-Vertriebsgesellschaft mbH & Co. KG
DE-MF-000006965 · Germany · Herne
Dr. Hinz Dental-Vertriebsgesellschaft mbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 60 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 60 |
|---|
Most frequent device types declared: Bruxi+, Friedensstifter®, IST®, IST®-Bissgabel, Lamtiec® Folien.
Devices declared under this manufacturer
- Bruxi+, einzeln
- Friedensstifter® KL I
- Friedensstifter® KL II
- ISTplus®-Set n. Prof. Hinz, Folien Ø 120
- ISTplus®-Set n. Prof. Hinz, LAMItec® Ø125
- IST®-Bissgabel n. Prof. Hinz
- IST®classic-Set n. Prof. Hinz, Teleskope (HF15), Folien Ø125
- Labor-Set Ø 125 (L1:0,5,L2:1,8)
- Laminierfolie Einführungs-Set Ø 125 (L1:0,5,L2:1,8)
- Muppy Perle II transparent/starr
- Muppy Käppchen II, transparent/starr
- OrthoPreventAligner® PR-W soft
Showing 12 of 60 declared devices.
Catalogue references include 90931, 90981, 90984, 97408, 97451, 98045.
European nomenclature codes declared: Q010499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 60 |
| 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 | 60 |
|---|---|
| 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. Dr. Hinz Dental-Vertriebsgesellschaft mbH & Co. KG was not found in either the U.S. or the Canadian register.