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

FDA-registered makers of Intervertebral Fusion Device With Bone Graft, Lumbar in Switzerland: 19 establishments

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

19 establishments in Switzerland are registered with the FDA to make Intervertebral Fusion Device With Bone Graft, Lumbar (product code MAX). 10 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 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 Switzerland Watch these makers

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

Makers of Intervertebral Fusion Device With Bone Graft, Lumbar in Switzerland

Maker	Location	Role	510(k) clearances	Latest clearance	PMA approvals	Recall events	Source
Medos International Sarl	Le Locle Neuchatel, Switzerland	Specification developer	21	March 8, 2023	0	0	api.fda.gov
Spineart SA	Plan-les-Ouates, Switzerland	Complaint file establishment, Specification developer	14	August 20, 2026	0	1	api.fda.gov
Medacta International SA	Castel San Pietro Ticino, Switzerland	Complaint file establishment, Manufacturer	9	July 17, 2025	0	0	api.fda.gov
Medacta International SA	Rancate Ticino, Switzerland	Complaint file establishment, Manufacturer	9	July 17, 2025	0	0	api.fda.gov
Synthes GMBH	Zuchwil Solothurn, Switzerland	Specification developer	6	December 6, 2018	0	0	api.fda.gov
Synthes GMBH	Selzach Solothurn, Switzerland	Manufacturer	5	December 6, 2018	1	0	api.fda.gov
Neo Medical S.A.	Villette (Lavaux) Vaud, Switzerland	Specification developer	2	December 13, 2019	0	0	api.fda.gov
Coligne AG	Zurich, Switzerland	Manufacturer	1	November 14, 2018	0	0	api.fda.gov
Getset Surgical S.A.	Epalinges Vaud, Switzerland	Complaint file establishment, Specification developer	1	March 21, 2025	0	0	api.fda.gov
Icotec AG	Altstaetten Sankt Gallen, Switzerland	Complaint file establishment, Manufacturer	1	April 5, 2024	0	0	api.fda.gov
Frueh Verpackungstechnik AG	Fehraltorf Zurich, Switzerland	Contract manufacturer	0		0	0	api.fda.gov
Gsell Medical Plastics AG	Muri Aargau, Switzerland	Contract manufacturer	0		0	0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Hagendorf)	Hagendorf Solothurn, Switzerland	Contract manufacturer	0		0	0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Le Locle)	Le Locle Neuchatel, Switzerland	Contract manufacturer	0		0	0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Mezzovico)	Mezzovico Ticino, Switzerland	Contract manufacturer	0		0	0	api.fda.gov
Leitner AG	Busswil Bern, Switzerland	Contract manufacturer	0		0	0	api.fda.gov
Moser-Baer AG	Sumiswald Bern, Switzerland	Contract manufacturer	0		0	0	api.fda.gov
Orchid Orthopedics Switzerland GMBH	Baden-Daettwil Aargau, Switzerland	Contract manufacturer	0		0	0	api.fda.gov
Ruetschi Technology AG	Muntelier Fribourg, Switzerland	Contract manufacturer	0		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.