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: 13014530, Idys® ALIF, Idys® C, Idys® TLIF, MONOAXIAL SCREW.
Among these devices, 26 are declared sterile, 399 implantable, 492 reusable, 492 active.
Devices declared under this manufacturer
- BROCHE (Ø1,5 MM - LG 500 MM)
- CAGE TLIF (W29 D11 H11 MM)
- CURETTE CUILLÈRE (H 05 MM)
- ERISMA-LP NAV TAP D7.5MM
- PINCE A DISQUE INCLINEE A 30° (6 MM - LG320MM)
- PINCE DE COMPRESSION
- POUSSE TIGE
- TARAUD (Ø 8,5 MM)
- TARAUD (Ø4,5 MM)
- TARAUD CANULE (Ø 9,5 MM)
- VIS POLYAXIALE (Ø 8,5 MM L 60 MM)
- VIS POLYAXIALE CANULEE MIS ( Ø 4,5 MM L 40 MM )
Showing 12 of 891 declared devices.
Catalogue references include 04704005, 06532911-S, 13014540, 13028560, 18158560, 50701045.
European nomenclature codes declared: P090799, P09070302, P09070101.
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 |
Device-level evidence
| Devices with a numeric GTIN | 891 |
|---|---|
| Found in the U.S. device database | 642 |
| Share | 72.1 % |
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: United States only. Clariance is registered in the United States but was not found in the Canadian register.