Data / Medical devices / Spinal Vertebral Body Replacement Device / Switzerland
FDA-registered makers of Spinal Vertebral Body Replacement Device in Switzerland: 11 establishments
11 establishments in Switzerland are registered with the FDA to make Spinal Vertebral Body Replacement Device (product code MQP). 5 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
- Spinal Vertebral Body Replacement Device
- Product code
- MQP
- Country
- Switzerland
Makers of Spinal Vertebral Body Replacement Device in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Synthes GMBH | Zuchwil Solothurn, Switzerland | Specification developer | 11 | May 23, 2019 | 0 | 0 | 0 | api.fda.gov |
| Medos International Sarl | Le Locle Neuchatel, Switzerland | Specification developer | 8 | June 11, 2018 | 0 | 0 | 0 | api.fda.gov |
| Synthes GMBH | Selzach Solothurn, Switzerland | Manufacturer | 7 | June 11, 2018 | 0 | 0 | 0 | api.fda.gov |
| Icotec AG | Altstaetten Sankt Gallen, Switzerland | Complaint file establishment, Manufacturer | 2 | April 4, 2024 | 0 | 0 | 0 | api.fda.gov |
| Coligne AG | Zurich, Switzerland | Manufacturer | 1 | June 24, 2008 | 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 (Grenchen) | Grenchen Solothurn, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jabil Switzerland Manufacturing GmbH (Hagendorf) | Hagendorf Solothurn, 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 | |
| Jabil Switzerland Manufacturing GmbH (Mezzovico) | Mezzovico Ticino, 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.