LSO Medical
FR-MF-000009080 · France · Loos
LSO Medical 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 IIb | 6 |
|---|---|
| Class IIa | 8 |
Among these devices, 8 are declared sterile, 6 active.
Catalogue references include ORLF000003, ORLF000005_SB, ORLF000006, ORLF000007, ORLF000007_SB, PHARAON1470.
European nomenclature codes declared: Z12011085, Z12011016.
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. LSO Medical was not found in either the U.S. or the Canadian register.