Data / Medical devices / Neurological Stereotaxic Instrument / France
FDA-registered makers of Neurological Stereotaxic Instrument in France: 7 establishments
7 establishments in France are registered with the FDA to make Neurological Stereotaxic Instrument (product code HAW). 3 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
- Neurological Stereotaxic Instrument
- Product code
- HAW
- Country
- France
Makers of Neurological Stereotaxic Instrument in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medtech SAS | MAUGUIO Occitanie, France | Manufacturer | 3 | July 20, 2023 | 0 | 4 | 2 | api.fda.gov |
| Blue Ortho | Meylan Isere, France | Manufacturer | 1 | July 13, 2016 | 0 | 0 | 0 | api.fda.gov |
| Renishaw Mayfield | Chassieu Rhone, France | Manufacturer | 1 | July 26, 2018 | 0 | 0 | 0 | api.fda.gov |
| Euclide Care | Aixe Sur Vienne Haute-Vienne, 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.