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Data / Medical devices / Instrument, Surgical, Non-Powered / France

FDA-registered makers of Instrument, Surgical, Non-Powered in France: 8 establishments

8 establishments in France are registered with the FDA to make Instrument, Surgical, Non-Powered (product code HAO). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Instrument, Surgical, Non-Powered
Product code
HAO
Country
France

Makers of Instrument, Surgical, Non-Powered in France

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Dixi MedicalMARCHAUX-CHAUDEFONTAINE Doubs, FranceComplaint file establishment, Manufacturer0000api.fda.gov
In'tech Medical SASRANG DU FLIERS Pas-de-Calais, FranceContract manufacturer, Exporter to the US0000api.fda.gov
MIP-plasticVilleneuve-en-Perseigne Sarthe, FranceContract manufacturer0000api.fda.gov
Oury-Guye & FilsNOGENT Haute-Marne, FranceContract manufacturer0000api.fda.gov
Stryker SpineCESTAS Nouvelle-Aquitaine, FranceContract manufacturer0000api.fda.gov
Symmetry Medical Polyvac SASWAMBRECHIES Nord, FranceContract manufacturer0000api.fda.gov
Tissium SARoncq Nord, FranceManufacturer0000api.fda.gov
Tissium SAParis 20e Arrondissement, FranceComplaint file establishment, Specification developer0000api.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.