Data / Medical devices / Spinal Vertebral Body Replacement Device / France
FDA-registered makers of Spinal Vertebral Body Replacement Device in France: 13 establishments
13 establishments in France are registered with the FDA to make Spinal Vertebral Body Replacement Device (product code MQP). 2 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
- Spinal Vertebral Body Replacement Device
- Product code
- MQP
- Country
- France
Makers of Spinal Vertebral Body Replacement Device 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 | 8 | May 16, 2017 | 0 | 0 | 0 | api.fda.gov |
| Spinevision SAS | Antony Hauts-de-Seine, France | Complaint file establishment, Manufacturer | 1 | December 28, 2004 | 0 | 0 | 0 | api.fda.gov |
| A.F.T. Micromecanique | Fillinges 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 | |
| Coulot Decolletage | CHATELLERAULT Vienne, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lopitz Manufacturing | Gradignan Nouvelle-Aquitaine, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oury-Guye & Fils | NOGENT Haute-Marne, 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 | |
| Sferic | MENARS Centre-Val de Loire, 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 | |
| Symmetry Medical Polyvac SAS | WAMBRECHIES Nord, 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.