NEOORTHOPEDIE
FR-MF-000038032 · France · Les Pennes Mirabeau
NEOORTHOPEDIE is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Devices declared under this manufacturer
- NEOFOOT D40
- NEOFOOT D60
- NEOFOOT G40
- NEOFOOT G60
- barre 21
- barre 24
- barre 27
- barre 30
- languette NEOFOOT
Catalogue references include NEO2023NFB21, NEO2023NFB27, NEO2023NFB30, NEO2023NFD40, NEO2023NFD60, NEO2023NFG40.
European nomenclature codes declared: Y0699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| 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 | 9 |
|---|---|
| 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. NEOORTHOPEDIE was not found in either the U.S. or the Canadian register.