Data / Medical devices / Intervertebral Fusion Device With Bone Graft, Lumbar / France

FDA-registered makers of Intervertebral Fusion Device With Bone Graft, Lumbar in France: 21 establishments

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

21 establishments in France are registered with the FDA to make Intervertebral Fusion Device With Bone Graft, Lumbar (product code MAX). 6 have a 510(k) clearance or PMA approval on file and 1 has 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.

Get makers of this device in France Watch these makers

Device: Intervertebral Fusion Device With Bone Graft, Lumbar
Product code: MAX
Country: France

Makers of Intervertebral Fusion Device With Bone Graft, 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	6	December 31, 2024	0	api.fda.gov
Spinevision SAS	Antony Hauts-de-Seine, France	Complaint file establishment, Manufacturer	4	December 16, 2022	0	api.fda.gov
LDR Medical	Sainte-Savine Aube, France	Specification developer	3	March 31, 2016	0	api.fda.gov
Medicrea International	RILLIEUX-LA-PAPE Auvergne-Rhone-Alpes, France	Manufacturer	2	September 6, 2024	3	api.fda.gov
Safe Orthopaedics SAS	Fleurieux-Sur-L'Arbresle Rhone, France	Manufacturer	2	March 14, 2014	0	api.fda.gov
Implanet	Martillac Nouvelle-Aquitaine, France	Manufacturer	1	February 26, 2026	0	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
Coulot Decolletage	CHATELLERAULT Vienne, 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
Selenium Medical S.A.S.	La Rochelle Charente-Maritime, France	Contract manufacturer	0		0	api.fda.gov
Sferic	MENARS Centre-Val de Loire, France	Contract manufacturer	0		0	api.fda.gov
Simagec	ROUSSET CEDEX Bouches-du-Rhone, France	Contract manufacturer	0		0	api.fda.gov
Simon SAS	Bayeux Calvados, France	Contract manufacturer	0		0	api.fda.gov
Stryker Spine	CESTAS Nouvelle-Aquitaine, France	Contract manufacturer	0		0	api.fda.gov
Symmetry Medical Polyvac SAS	WAMBRECHIES Nord, France	Contract manufacturer	0		0	api.fda.gov
Safe Medical	Fleurieux-Sur-L'Arbresle Rhone, France	Contract manufacturer	0		0	api.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.