Clariance
FR-MF-000023666 · France · Beaurains
Clariance is registered in the European database on medical devices as a manufacturer, with 891 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 492 |
|---|---|
| Class IIb | 399 |
Most frequent device types declared: Spinal instrumentation, Pedicle screw, Idys® ALIF, Idys® TLIF, Idys® C.
Among these devices, 26 are declared sterile, 399 implantable, 492 reusable, 492 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 | CLARIANCE-SAS (FR) · FDA 3008992889 |
| Devices in EUDAMED | 891 |
| Country of registration | France |