Fesia technology
ES-MF-000004643 · Spain · Donostia/San Sebastian
Fesia technology is registered in the European database on medical devices as a manufacturer, with 48 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 48 |
|---|
Among these devices, 48 are declared reusable, 48 active.
Devices declared under this manufacturer
- Fesia Bike Pro Active Nuro
- Fesia Electrode Arm Elbow GB Unique/Size Unique/2
- Fesia Electrode Arm Elbow Right/Size Unique/2
- Fesia Electrode Forearm Right/Size Medium-Large
- Fesia Electrode Gluteus Add-on Unique/Size Unique/2
- Fesia Electrode Shank GB Left/Size Unique/2
- Fesia Electrode Shank GB Right/Size Unique/2/MN2
- Fesia Electrode Shank Left/Size Unique/1
- Fesia Electrode Thigh Left/Size Unique/2
- Fesia Grasp Active + Left/Size Medium-Large
- Fesia Grasp Active Right/Size Small-Medium
- Fesia Grasp Pro
Showing 12 of 48 declared devices.
Catalogue references include ELAE-RU2, ELFR-RM, ELGL-AUU2, ELSH-GB-LU2, ELTH-LU2, STGA.G10.
European nomenclature codes declared: Z12062780, Z12062702, Z12062799, Z12062704, Z12062703.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 48 |
| Country of registration | Spain |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 48 |
|---|---|
| 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. Fesia technology was not found in either the U.S. or the Canadian register.