Data / Medical devices / Sterilization Wrap Containers, Trays, Cassettes & Other Accessories / Switzerland
FDA-registered makers of Sterilization Wrap Containers, Trays, Cassettes & Other Accessories in Switzerland: 9 establishments
9 establishments in Switzerland are registered with the FDA to make Sterilization Wrap Containers, Trays, Cassettes & Other Accessories (product code KCT). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
- Product code
- KCT
- Country
- Switzerland
Makers of Sterilization Wrap Containers, Trays, Cassettes & Other Accessories in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Nobel Biocare Services AG | Kloten Zurich, Switzerland | Specification developer | 5 | September 8, 2026 | 0 | 0 | 0 | api.fda.gov |
| Institut Straumann AG | BASEL Basel-Stadt, Switzerland | Complaint file establishment, Specification developer | 4 | June 3, 2026 | 0 | 0 | 0 | api.fda.gov |
| Synthes GMBH | Zuchwil Solothurn, Switzerland | Specification developer | 3 | March 28, 2025 | 0 | 0 | 0 | api.fda.gov |
| Straumann Villeret SA | VILLERET Bern, Switzerland | Manufacturer | 2 | July 29, 2021 | 0 | 0 | 0 | api.fda.gov |
| Infinetamed AG | Sarnen Obwalden, Switzerland | Complaint file establishment, Manufacturer, Specification developer | 1 | February 11, 2025 | 0 | 0 | 0 | api.fda.gov |
| Medos International Sarl | Le Locle Neuchatel, Switzerland | Specification developer | 1 | February 26, 2026 | 0 | 0 | 0 | api.fda.gov |
| Z-Systems AG | Oensingen Solothurn, Switzerland | Manufacturer | 1 | March 25, 2021 | 0 | 0 | 0 | api.fda.gov |
| Medartis AG | BASEL Basel-Stadt, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ringele AG | Pratteln Basel-Landschaft, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.