Data / Medical devices / Bone Cement, Posterior Screw Augmentation / Switzerland
FDA-registered makers of Bone Cement, Posterior Screw Augmentation in Switzerland: 10 establishments
10 establishments in Switzerland are registered with the FDA to make Bone Cement, Posterior Screw Augmentation (product code PML). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Bone Cement, Posterior Screw Augmentation
- Product code
- PML
- Country
- Switzerland
Makers of Bone Cement, Posterior Screw Augmentation in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Icotec AG | Altstaetten Sankt Gallen, Switzerland | Complaint file establishment, Manufacturer | 2 | January 9, 2023 | 0 | 1 | 0 | api.fda.gov |
| Neo Medical S.A. | Villette (Lavaux) Vaud, Switzerland | Specification developer | 2 | August 26, 2022 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Castel San Pietro Ticino, Switzerland | Complaint file establishment, Manufacturer | 1 | June 12, 2024 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Rancate Ticino, Switzerland | Complaint file establishment, Manufacturer | 1 | June 12, 2024 | 0 | 0 | 0 | api.fda.gov |
| Medos International Sarl | Le Locle Neuchatel, Switzerland | Specification developer | 1 | December 20, 2016 | 0 | 0 | 0 | api.fda.gov |
| Spineart SA | Plan-les-Ouates, Switzerland | Complaint file establishment, Specification developer | 1 | June 23, 2023 | 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 | |
| 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.