Data / Medical devices / Intervertebral Fusion Device With Integrated Fixation, Cervical / France
FDA-registered makers of Intervertebral Fusion Device With Integrated Fixation, Cervical in France: 16 establishments
16 establishments in France are registered with the FDA to make Intervertebral Fusion Device With Integrated Fixation, Cervical (product code OVE). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Intervertebral Fusion Device With Integrated Fixation, Cervical
- Product code
- OVE
- Country
- France
Makers of Intervertebral Fusion Device With Integrated Fixation, Cervical in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Clariance-Sas | BEAURAINS Hauts-de-France, France | Complaint file establishment, Manufacturer, Specification developer | 2 | March 22, 2024 | 0 | 0 | 0 | api.fda.gov |
| LDR Medical | Sainte-Savine Aube, France | Specification developer | 2 | December 7, 2015 | 0 | 0 | 0 | api.fda.gov |
| Safe Orthopaedics SAS | Fleurieux-Sur-L'Arbresle Rhone, France | Manufacturer | 2 | January 10, 2022 | 0 | 0 | 0 | api.fda.gov |
| Spinevision SAS | Antony Hauts-de-Seine, France | Complaint file establishment, Manufacturer | 2 | November 14, 2022 | 0 | 0 | 0 | api.fda.gov |
| Medicrea International | RILLIEUX-LA-PAPE Auvergne-Rhone-Alpes, France | Manufacturer | 1 | September 3, 2021 | 0 | 0 | 0 | api.fda.gov |
| 3D Medical SAS | Marolles en Brie Val-de-Marne, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| A.F.T. Micromecanique | Fillinges Haute-Savoie, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alpes CN SAS | Reignier-Esery Haute-Savoie, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Anthogyr | SALLANCHES Haute-Savoie, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cefimeca | La Talaudiere Loire, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Charles Pery & Cie | SCIONZIER Haute-Savoie, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Coulot Decolletage | CHATELLERAULT Vienne, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Precera Medical Neyron SAS | MIRIBEL CEDEX Auvergne-Rhone-Alpes, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Selenium Medical S.A.S. | La Rochelle Charente-Maritime, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Simagec | ROUSSET CEDEX Bouches-du-Rhone, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Spine | CESTAS Nouvelle-Aquitaine, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.