SpineSave AG
CH-MF-000041640 · Switzerland · Embrach
SpineSave AG is registered in the European database on medical devices as a manufacturer, with 31 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 31 |
|---|
Among these devices, 31 are declared reusable.
Authorised representative in the Union: SpineSave GmbH.
Devices declared under this manufacturer
- spineshape
Showing 12 of 31 declared devices.
Catalogue references include 20.001.03, 20.001.10/11, 20.004.00, 20.005.20, 20.006.00, 20.006.31.
European nomenclature codes declared: L091104, L098003, L091103, L0922, L99, L091102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 31 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 31 |
|---|---|
| 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. SpineSave AG was not found in either the U.S. or the Canadian register.