Data / Medical devices / Dispenser, Cement / Switzerland
FDA-registered makers of Dispenser, Cement in Switzerland: 6 establishments
6 establishments in Switzerland are registered with the FDA to make Dispenser, Cement (product code KIH). 0 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
- Dispenser, Cement
- Product code
- KIH
- Country
- Switzerland
Makers of Dispenser, Cement 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 | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neo Medical S.A. | Villette (Lavaux) Vaud, Switzerland | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ruetschi Technology AG | Muntelier Fribourg, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spineart SA | Plan-les-Ouates, Switzerland | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Synthes GMBH | Zuchwil Solothurn, Switzerland | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Synthes GMBH | Selzach Solothurn, Switzerland | 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.