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Data / Medical devices / Extractor / France

FDA-registered makers of Extractor in France: 9 establishments

9 establishments in France are registered with the FDA to make Extractor (product code HWB). 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
Extractor
Product code
HWB
Country
France

Makers of Extractor in France

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
AmplitudeValence Drome, FranceComplaint file establishment, Manufacturer0000api.fda.gov
CefimecaLa Talaudiere Loire, FranceContract manufacturer0000api.fda.gov
In'tech Medical SASRANG DU FLIERS Pas-de-Calais, FranceContract manufacturer, Exporter to the US0000api.fda.gov
Maire-DidierChaumont Haute-Marne, FranceContract manufacturer0000api.fda.gov
Medical GroupSAINT-PRIEST Auvergne-Rhone-Alpes, FranceContract manufacturer0000api.fda.gov
Medicrea InternationalRILLIEUX-LA-PAPE Auvergne-Rhone-Alpes, FranceManufacturer0000api.fda.gov
MicrotechnicCROLLES Isere, FranceContract manufacturer0000api.fda.gov
Tornier S.A.S.Montbonnot Saint-Martin Isere, FranceComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Viant Chaumont S.A.S.CHAUMONT Haute-Marne, FranceContract 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.