Data / Medical devices / Posterior Cervical Screw System / Switzerland
FDA-registered makers of Posterior Cervical Screw System in Switzerland: 13 establishments
13 establishments in Switzerland are registered with the FDA to make Posterior Cervical Screw System (product code NKG). 7 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
- Posterior Cervical Screw System
- Product code
- NKG
- Country
- Switzerland
Makers of Posterior Cervical Screw System in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medos International Sarl | Le Locle Neuchatel, Switzerland | Specification developer | 7 | November 9, 2023 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Castel San Pietro Ticino, Switzerland | Complaint file establishment, Manufacturer | 6 | April 26, 2022 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Rancate Ticino, Switzerland | Complaint file establishment, Manufacturer | 6 | April 26, 2022 | 0 | 0 | 0 | api.fda.gov |
| Synthes GMBH | Zuchwil Solothurn, Switzerland | Specification developer | 4 | April 2, 2020 | 0 | 0 | 0 | api.fda.gov |
| Synthes GMBH | Selzach Solothurn, Switzerland | Manufacturer | 4 | July 18, 2019 | 0 | 0 | 0 | api.fda.gov |
| Spineart SA | Plan-les-Ouates, Switzerland | Complaint file establishment, Specification developer | 3 | May 1, 2020 | 0 | 0 | 0 | api.fda.gov |
| Icotec AG | Altstaetten Sankt Gallen, Switzerland | Complaint file establishment, Manufacturer | 1 | November 12, 2025 | 0 | 0 | 0 | api.fda.gov |
| Boillat Decolletage SA | Loveresse Bern, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Frueh Verpackungstechnik AG | Fehraltorf Zurich, 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 | |
| Leitner AG | Busswil Bern, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wymed Precision Mechanics | Embrach Zurich, 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.