Data / Medical devices / Orthopedic Stereotaxic Instrument / France
FDA-registered makers of Orthopedic Stereotaxic Instrument in France: 12 establishments
12 establishments in France are registered with the FDA to make Orthopedic Stereotaxic Instrument (product code OLO). 4 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Orthopedic Stereotaxic Instrument
- Product code
- OLO
- Country
- France
Makers of Orthopedic Stereotaxic Instrument in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Blue Ortho | Meylan Isere, France | Manufacturer | 8 | January 26, 2024 | 0 | 2 | 0 | api.fda.gov |
| Ecential Robotics | Gieres Isere, France | Manufacturer | 4 | July 22, 2026 | 0 | 0 | 0 | api.fda.gov |
| Clariance-Sas | BEAURAINS Hauts-de-France, France | Complaint file establishment, Manufacturer, Specification developer | 1 | February 26, 2021 | 0 | 0 | 0 | api.fda.gov |
| Euclide Care | Aixe Sur Vienne Haute-Vienne, France | Contract manufacturer, Exporter to the US | 1 | October 18, 2017 | 0 | 0 | 0 | api.fda.gov |
| Alpes CN SAS | Reignier-Esery 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 | |
| Dubourgel Grange | Fontaine Isere, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| In'tech Medical SAS | RANG DU FLIERS Pas-de-Calais, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtech SAS | MAUGUIO Occitanie, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microtechnic | CROLLES Isere, 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.