Data / Medical devices / Intervertebral Fusion Device With Integrated Fixation, Lumbar / France

FDA-registered makers of Intervertebral Fusion Device With Integrated Fixation, Lumbar in France: 12 establishments

Name: FDA-registered makers of Intervertebral Fusion Device With Integrated Fixation, Lumbar in France
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

12 establishments in France are registered with the FDA to make Intervertebral Fusion Device With Integrated Fixation, Lumbar (product code OVD). 3 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: Intervertebral Fusion Device With Integrated Fixation, Lumbar
Product code: OVD
Country: France

Makers of Intervertebral Fusion Device With Integrated Fixation, Lumbar in France

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Clariance-Sas	BEAURAINS Hauts-de-France, France	Complaint file establishment, Manufacturer, Specification developer	4	April 1, 2021	0	api.fda.gov
LDR Medical	Sainte-Savine Aube, France	Specification developer	4	September 28, 2016	0	api.fda.gov
Medicrea International	RILLIEUX-LA-PAPE Auvergne-Rhone-Alpes, France	Manufacturer	1	January 15, 2015	1	api.fda.gov
3D Medical SAS	Marolles en Brie Val-de-Marne, France	Contract manufacturer	0		0	api.fda.gov
A.F.T. Micromecanique	Fillinges Haute-Savoie, France	Contract manufacturer	0		0	api.fda.gov
Alpes CN SAS	Reignier-Esery Haute-Savoie, France	Contract manufacturer	0		0	api.fda.gov
Anthogyr	SALLANCHES Haute-Savoie, France	Contract manufacturer	0		0	api.fda.gov
Cefimeca	La Talaudiere Loire, France	Contract manufacturer	0		0	api.fda.gov
Euclide Care	Aixe Sur Vienne Haute-Vienne, 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
Simagec	ROUSSET CEDEX Bouches-du-Rhone, France	Contract manufacturer	0		0	api.fda.gov
Stryker Spine	CESTAS Nouvelle-Aquitaine, 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.