Data / Medical devices / Plate, Fixation, Bone / France

FDA-registered makers of Plate, Fixation, Bone in France: 20 establishments

Name: FDA-registered makers of Plate, Fixation, Bone in France
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

20 establishments in France are registered with the FDA to make Plate, Fixation, Bone (product code HRS). 6 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: Plate, Fixation, Bone
Product code: HRS
Country: France

Makers of Plate, Fixation, Bone in France

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Newclip Technics SAS	HAUTE GOULAINE Loire-Atlantique, France	Manufacturer	26	September 28, 2026	0	api.fda.gov
Biomet France	Valence Drome, France	Manufacturer	17	April 6, 2018	0	api.fda.gov
Novastep	RENNES Bretagne, France	Manufacturer	4	March 25, 2026	0	api.fda.gov
Fx Shoulder Solutions SAS	Viriat Auvergne-Rhone-Alpes, France	Manufacturer, Specification developer	1	August 27, 2015	0	api.fda.gov
In2Bones SAS	Saint-Priest Rhone, France	Exporter to the US, Specification developer	1	November 28, 2017	2	api.fda.gov
Science & Bio Materials, S.B.M. SAS	LOURDES Hautes-Pyrenees, France	Complaint file establishment, Manufacturer	1	April 19, 2012	0	api.fda.gov
Charles Pery & Cie	SCIONZIER Haute-Savoie, France	Contract manufacturer	0		0	api.fda.gov
Clayens Genas	Genas Rhone, France	Contract manufacturer	0		0	api.fda.gov
Coulot Decolletage	CHATELLERAULT Vienne, France	Contract manufacturer	0		0	api.fda.gov
In'tech Medical SAS	RANG DU FLIERS Pas-de-Calais, France	Contract manufacturer	0		0	api.fda.gov
Marle Finishing SAS	La Talaudiere Loire, France	Contract manufacturer	0		0	api.fda.gov
Medical Group	SAINT-PRIEST Auvergne-Rhone-Alpes, France	Contract manufacturer	0		0	api.fda.gov
Medicatechnologie	CHARTRES-DE-BRETAGNE Ille-et-Vilaine, France	Contract manufacturer	0		0	api.fda.gov
Phen'x Technologies	Chassieu Auvergne-Rhone-Alpes, France	Contract manufacturer	0		0	api.fda.gov
Precera Medical Herouville SAS	HEROUVILLE ST CLAIR CEDEX Normandie, France	Contract manufacturer	0		0	api.fda.gov
Precera Medical Neyron SAS	MIRIBEL CEDEX Auvergne-Rhone-Alpes, France	Contract manufacturer	0		0	api.fda.gov
Selenium Medical S.A.S.	La Rochelle Charente-Maritime, France	Contract manufacturer	0		0	api.fda.gov
Simagec	ROUSSET CEDEX Bouches-du-Rhone, France	Contract manufacturer	0		0	api.fda.gov
Symmetry Medical Polyvac SAS	WAMBRECHIES Nord, France	Contract manufacturer	0		0	api.fda.gov
Societe Marnaise D'Applications Orthopediques (SMAO) Sarl	Villiers Le Sec Haute-Marne, France	Contract manufacturer	0		0	api.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.