Data / Medical devices / Intervertebral Fusion Device With Bone Graft, Cervical / France
FDA-registered makers of Intervertebral Fusion Device With Bone Graft, Cervical in France: 14 establishments
14 establishments in France are registered with the FDA to make Intervertebral Fusion Device With Bone Graft, Cervical (product code ODP). 4 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Intervertebral Fusion Device With Bone Graft, Cervical
- Product code
- ODP
- Country
- France
Makers of Intervertebral Fusion Device With Bone Graft, Cervical in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| LDR Medical | Sainte-Savine Aube, France | Specification developer | 2 | December 29, 2011 | 0 | 0 | 0 | api.fda.gov |
| Clariance-Sas | BEAURAINS Hauts-de-France, France | Complaint file establishment, Manufacturer, Specification developer | 1 | November 13, 2013 | 0 | 0 | 0 | api.fda.gov |
| Implanet | Martillac Nouvelle-Aquitaine, France | Manufacturer | 1 | March 28, 2023 | 0 | 0 | 0 | api.fda.gov |
| Medicrea International | RILLIEUX-LA-PAPE Auvergne-Rhone-Alpes, France | Manufacturer | 1 | March 16, 2010 | 0 | 1 | 0 | api.fda.gov |
| 3D Medical SAS | Marolles en Brie Val-de-Marne, 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 | |
| Coulot Decolletage | CHATELLERAULT Vienne, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Safe Orthopaedics SAS | Fleurieux-Sur-L'Arbresle Rhone, France | 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 | |
| Safe Medical | Fleurieux-Sur-L'Arbresle Rhone, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.