L-Force Oy
FI-MF-000006911 · Finland · Helsinki
L-Force Oy is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Among these devices, 6 are declared active.
Devices declared under this manufacturer
- RADU v.16.0
- Radu RIS v.17.0
- Radu RIS v.18.0
- Radu RIS v.19.0
- Radu RIS v.20.0.3
- Radu RIS v.20.1
Catalogue references include 06429810604002, 06429810604019, 06429810604026, 06429810604033, 06429810604040, 06429810604057.
European nomenclature codes declared: Z119082.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| 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. L-Force Oy was not found in either the U.S. or the Canadian register.