Millet Innovation
FR-MF-000004611 · France · Loriol Sur Drôme
Millet Innovation is registered in the European database on medical devices as a manufacturer, with 339 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 339 |
|---|
Devices declared under this manufacturer
- Chevillère ligamentaire
- Coussinets Plantaires
- Enkelknobbel beschermer SPORT
- Genouillère ligamentaire
- HALLUX Corrigerende ORTHOSIS SPORT Large
- HALLUX Corrigerende ORTHOSIS SPORT Medium
- Ortesi correttiva doppia da giorno Alluce Valgo \
- Orthèse corrective double de jour Hallux Valgus \
- Orthèse pouce rigide de nuit Rhizarthrose
- PROTEZIONE COMFORT QUINTUS VARUS EPITACT
- Physio'chocTM - Kantapäätyyny / Physio'chocTM - Hälkudde
- Protection anti-ampoules à l'Epithelium
Showing 12 of 339 declared devices.
Catalogue references include 0531GD, 0531GIT, 0581G, CC2612, G502NL, G710NL.
European nomenclature codes declared: Y99, Y061203, Y06120601, Y060613, Y061209, Y060612.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 339 |
| 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 | 339 |
|---|---|
| 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. Millet Innovation was not found in either the U.S. or the Canadian register.