GÖCKENER GMBH
DE-MF-000009282 · Germany · Ahaus
GÖCKENER GMBH is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 25 |
|---|
Devices declared under this manufacturer
- AOK Kalt/Warm Kompresse für Merfachanwendung
- APOGEPHA Ultraschallgel
- DORNBACH Moor-Wärmekissen
- ELBLANDKLINIKEN Kompresse für Mehfachanwendung
- Ergosia Kalt/Warm Kompresse
- GALDERMA, Restylane, SCULPTRA Kühlkompresse
- JAWLAX WÄRMEKISSEN
- MERZ AESTHETICS Kalt/Warm Kompresse
- MERZ AESTHETICS Kalt/Warm Kompressen für Mehrfachanwendungen
- ORAL & KIEFERSCHIRURGIE BRAUNSCHWEIG
- SPORLASTIC Kalt-/Warmkompresse
- ULTRASONIC GEL for Skinova
Showing 12 of 25 declared devices.
Catalogue references include 000250731, 000250745, 000250746, 075140710, 100120729, 107115701.
European nomenclature codes declared: M9001, Z11040185.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 25 |
| 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 | 25 |
|---|---|
| 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. GÖCKENER GMBH was not found in either the U.S. or the Canadian register.