FTA
FR-MF-000047307 · France · LE CRES
FTA is registered in the European database on medical devices as a manufacturer, with 30 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 30 |
|---|
Most frequent device types declared: Montures Cerclées en Plastique.
Catalogue references include CM-A37, CM-A39, CM-A48, CM-A50, CM-A54, CM-A56.
European nomenclature codes declared: Q02100202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 30 |
| 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 | 30 |
|---|---|
| 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. FTA was not found in either the U.S. or the Canadian register.