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Data / Medical devices / Retractor / France

FDA-registered makers of Retractor in France: 16 establishments

16 establishments in France are registered with the FDA to make Retractor (product code GAD). 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
Retractor
Product code
GAD
Country
France

Makers of Retractor in France

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
AmplitudeValence Drome, FranceComplaint file establishment, Manufacturer0000api.fda.gov
Askorn MedicalCesson Sevigne Bretagne, FranceExporter to the US, Specification developer0000api.fda.gov
Biomet FranceValence Drome, FranceManufacturer0000api.fda.gov
CefimecaLa Talaudiere Loire, FranceContract manufacturer0000api.fda.gov
Clariance-SasBEAURAINS Hauts-de-France, FranceComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Euclide CareAixe Sur Vienne Haute-Vienne, FranceContract manufacturer, Exporter to the US0000api.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 relabeler0000api.fda.gov
LandangerCHAUMONT Haute-Marne, FranceManufacturer0000api.fda.gov
LDR MedicalSainte-Savine Aube, FranceSpecification developer0000api.fda.gov
Oury-Guye & FilsNOGENT Haute-Marne, FranceContract manufacturer0000api.fda.gov
Prince Medical SASERCUIS Oise, FranceManufacturer0000api.fda.gov
Spinevision SASAntony Hauts-de-Seine, FranceComplaint file establishment, Manufacturer0000api.fda.gov
Symmetry Medical Polyvac SASWAMBRECHIES Nord, FranceContract manufacturer0000api.fda.gov
Top Clean InjectionPESCHADOIRES Puy-de-Dome, FranceContract manufacturer0000api.fda.gov
Tornier S.A.S.Montbonnot Saint-Martin Isere, 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.