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Data / Medical devices / Driver, Prosthesis / France

FDA-registered makers of Driver, Prosthesis in France: 8 establishments

8 establishments in France are registered with the FDA to make Driver, Prosthesis (product code HWR). 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
Driver, Prosthesis
Product code
HWR
Country
France

Makers of Driver, Prosthesis in France

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
AmplitudeValence Drome, FranceComplaint file establishment, Manufacturer0000api.fda.gov
CefimecaLa Talaudiere Loire, FranceContract manufacturer0000api.fda.gov
Clariance-SasBEAURAINS Hauts-de-France, FranceComplaint file establishment, Manufacturer0000api.fda.gov
In'tech Medical SASRANG DU FLIERS Pas-de-Calais, FranceContract manufacturer, Exporter to the US0000api.fda.gov
Integra Microfrance SASSAINT AUBIN LE MONIAL Auvergne-Rhone-Alpes, FranceManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
In2Bones SASSaint-Priest Rhone, FranceExporter to the US, Specification developer0000api.fda.gov
Phen'x TechnologiesChassieu Auvergne-Rhone-Alpes, FranceContract manufacturer0000api.fda.gov
Spinevision SASAntony Hauts-de-Seine, FranceComplaint file establishment, Manufacturer0000api.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.