G-Pharma
FR-MF-000017094 · France · Herblay
G-Pharma is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 24 |
|---|
Most frequent device types declared: G-ETCH, Healbond, InnoCem, PHOENIX, Pureshade.
Devices declared under this manufacturer
- G-ETCH
- Healbond Max
- INNOCEM
- InnoCem
- PHOENIX
- PHOENIX MD
- Phoenix
- Pureshade
- SEALTEMP
- SEALTEMP S
- Seal Temp
- ULTIME ETCH
Showing 12 of 24 declared devices.
Catalogue references include ETG-16, IC-10 – TA2, JKV-50, JRB-50, JRV-50, PHMD-50-A1.
European nomenclature codes declared: Q01010402, Q0102050101, Q0101010203, Q0101010201, Q01010103, Q01010104.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 24 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 24 |
|---|---|
| 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. G-Pharma was not found in either the U.S. or the Canadian register.