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Data / Medical devices / Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented / France

FDA-registered makers of Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented in France: 12 establishments

12 establishments in France are registered with the FDA to make Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented (product code HSD). 2 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
Product code
HSD
Country
France

Makers of Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented in France

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Fx Shoulder Solutions SASViriat Auvergne-Rhone-Alpes, FranceComplaint file establishment, Manufacturer, Specification developer2November 9, 2013010api.fda.gov
Tornier S.A.S.Montbonnot Saint-Martin Isere, FranceComplaint file establishment, Contract manufacturer, Manufacturer, Specification developer1July 13, 2001000api.fda.gov
CefimecaLa Talaudiere Loire, FranceContract manufacturer0000api.fda.gov
FH IndustrieQUIMPER Finistere, FranceManufacturer0000api.fda.gov
Marle Finishing SASLa Talaudiere Loire, FranceContract manufacturer0000api.fda.gov
Medical GroupSAINT-PRIEST Auvergne-Rhone-Alpes, FranceContract manufacturer0000api.fda.gov
Precera Medical Herouville SASHEROUVILLE ST CLAIR CEDEX Normandie, FranceContract manufacturer0000api.fda.gov
PrecimadeBourg en Bresse Ain, FranceContract manufacturer0000api.fda.gov
Simon SASBayeux Calvados, FranceContract manufacturer0000api.fda.gov
Tornier S.A.SMontbonnot Saint-Martin Isere, FranceManufacturer0000api.fda.gov
Viant Chaumont S.A.S.CHAUMONT Haute-Marne, FranceContract manufacturer0000api.fda.gov
Westlake Plastics EuropeTOURCOING Nord, 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.