Data / Medical devices / Intervertebral Fusion Device With Bone Graft, Cervical / Switzerland
FDA-registered makers of Intervertebral Fusion Device With Bone Graft, Cervical in Switzerland: 13 establishments
13 establishments in Switzerland are registered with the FDA to make Intervertebral Fusion Device With Bone Graft, Cervical (product code ODP). 8 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Intervertebral Fusion Device With Bone Graft, Cervical
- Product code
- ODP
- Country
- Switzerland
Makers of Intervertebral Fusion Device With Bone Graft, Cervical in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Spineart SA | Plan-les-Ouates, Switzerland | Complaint file establishment, Specification developer | 10 | March 22, 2023 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Castel San Pietro Ticino, Switzerland | Complaint file establishment, Manufacturer | 3 | September 18, 2017 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Rancate Ticino, Switzerland | Complaint file establishment, Manufacturer | 3 | September 18, 2017 | 0 | 0 | 0 | api.fda.gov |
| Icotec AG | Altstaetten Sankt Gallen, Switzerland | Complaint file establishment, Manufacturer | 2 | March 20, 2020 | 0 | 0 | 0 | api.fda.gov |
| Coligne AG | Zurich, Switzerland | Manufacturer | 1 | December 1, 2017 | 0 | 0 | 0 | api.fda.gov |
| Medos International Sarl | Le Locle Neuchatel, Switzerland | Specification developer | 1 | April 26, 2012 | 0 | 0 | 0 | api.fda.gov |
| Synthes GMBH | Zuchwil Solothurn, Switzerland | Specification developer | 1 | May 25, 2012 | 0 | 0 | 0 | api.fda.gov |
| Synthes GMBH | Selzach Solothurn, Switzerland | Manufacturer | 1 | December 21, 2017 | 0 | 0 | 0 | api.fda.gov |
| Frueh Verpackungstechnik AG | Fehraltorf Zurich, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gsell Medical Plastics AG | Muri Aargau, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jabil Switzerland Manufacturing GmbH (Le Locle) | Le Locle Neuchatel, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Leitner AG | Busswil Bern, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Moser-Baer AG | Sumiswald Bern, Switzerland | Contract manufacturer | 0 | 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.