Solsius SAS
FR-MF-000041700 · France · Lille
Solsius SAS is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 14 |
|---|
Among these devices, 14 are declared active.
Catalogue references include INSOLE-T1, INSOLE-T2, INSOLE-T3, INSOLE-T3-R, INSOLE-T4, INSOLE-T4-L.
European nomenclature codes declared: Z12062602, V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 14 |
|---|---|
| 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. Solsius SAS was not found in either the U.S. or the Canadian register.