Data / Medical devices / Instrument, Manual, Surgical, General Use / France
FDA-registered makers of Instrument, Manual, Surgical, General Use in France: 11 establishments
11 establishments in France are registered with the FDA to make Instrument, Manual, Surgical, General Use (product code MDM). 0 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
- Instrument, Manual, Surgical, General Use
- Product code
- MDM
- Country
- France
Makers of Instrument, Manual, Surgical, General Use in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Axess Vision Technology | Joue Les Tours Indre-et-Loire, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Euclide Care | Aixe Sur Vienne Haute-Vienne, France | Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.fda.gov | |
| In'tech Medical SAS | RANG DU FLIERS Pas-de-Calais, France | Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.fda.gov | |
| Integra Microfrance SAS | SAINT AUBIN LE MONIAL Auvergne-Rhone-Alpes, France | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Landanger | CHAUMONT Haute-Marne, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Conteneur SAS | SAINT-SOUPPLETS Seine-et-Marne, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Z, S.A. | SAINT AVERTIN Indre-et-Loire, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Moria S.A. | MASSY Hauts-de-Seine, France | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Moria S.A | Bourbon l'Archambault Allier, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spineguard, SA | Vincennes Paris, France | 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.