Data / Medical devices / Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis / France
FDA-registered makers of Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis in France: 11 establishments
11 establishments in France are registered with the FDA to make Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis (product code OSH). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
- Product code
- OSH
- Country
- France
Makers of Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medicrea International | RILLIEUX-LA-PAPE Auvergne-Rhone-Alpes, France | Manufacturer | 2 | November 8, 2013 | 0 | 0 | 0 | api.fda.gov |
| Implanet | Martillac Nouvelle-Aquitaine, France | Manufacturer | 1 | October 10, 2013 | 0 | 0 | 0 | api.fda.gov |
| Alpes CN SAS | Reignier-Esery 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 | |
| Cousin Biotech | WERVICQ-SUD Nord, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Euclide Care | Aixe Sur Vienne Haute-Vienne, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microtec SAS | Serres Castet Pyrenees-Atlantiques, 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 | |
| Symmetry Medical Polyvac SAS | WAMBRECHIES Nord, 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.