Companion Spine France SAS
FR-MF-000013875 · France · MERIGNAC
Companion Spine France SAS is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 18 |
|---|
Among these devices, 13 are declared reusable.
Devices declared under this manufacturer
- DIAM, 10mm Template
- DIAM, 12mm Template
- DIAM, 14mm Template
- DIAM, Bi-Lateral Impactor
- DIAM, Crimper
- DIAM, Distractor, Small with Knob
- DIAM, Outer Case
- DIAM, Outer Case (alt inserter)
- DIAM, Outer Case Lid
- DIAM, Sicard Punch, Large
- DIAM, Sicard Punch, Small
- DIAM, Tissue Resector-Left
Showing 12 of 18 declared devices.
Catalogue references include CS001B0010, CS001B0012, CS001B0014, CS001B0022, CS001B0025, CS001B0026.
European nomenclature codes declared: L091199, S010399, L0901, L090999, L0999.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | COMPANION SPINE (FR) · FDA 3025435185 |
| Devices in EUDAMED | 18 |
| Country of registration | France |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 18 |
|---|---|
| Found in the U.S. device database | 18 |
| Share | 100.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.