Kinetec SAS
FR-MF-000000364 · France · Tournes
Kinetec SAS is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: Kinetec Optima S4, Centura.
Among these devices, 20 are declared active.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Kinetec SAS (FR) · FDA 8020836 |
| Devices in EUDAMED | 20 |
| Country of registration | France |