Data / Medical devices / System, Image Processing, Radiological / Switzerland
FDA-registered makers of System, Image Processing, Radiological in Switzerland: 11 establishments
11 establishments in Switzerland are registered with the FDA to make System, Image Processing, Radiological (product code LLZ). 9 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
- System, Image Processing, Radiological
- Product code
- LLZ
- Country
- Switzerland
Makers of System, Image Processing, Radiological 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 | 7 | December 8, 2023 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Castel San Pietro Ticino, Switzerland | Complaint file establishment, Manufacturer | 5 | April 23, 2025 | 0 | 0 | 0 | api.fda.gov |
| Medacta International SA | Rancate Ticino, Switzerland | Complaint file establishment, Manufacturer | 5 | April 23, 2025 | 0 | 0 | 0 | api.fda.gov |
| Customsurg AG | Zurich, Switzerland | Complaint file establishment, Manufacturer | 1 | July 7, 2025 | 0 | 0 | 0 | api.fda.gov |
| Naviswiss AG | Brugg Aargau, Switzerland | Manufacturer | 1 | October 5, 2021 | 0 | 0 | 0 | api.fda.gov |
| Pixmeo Sarl | Bernex Geneve, Switzerland | Manufacturer | 1 | August 20, 2010 | 0 | 0 | 0 | api.fda.gov |
| Specto Medical AG | Basel Basel-Stadt, Switzerland | Complaint file establishment, Manufacturer | 1 | January 14, 2025 | 0 | 0 | 0 | api.fda.gov |
| Storz Medical AG | TAEGERWILEN Thurgau, Switzerland | Manufacturer | 1 | March 18, 2010 | 0 | 0 | 0 | api.fda.gov |
| Swissmeda AG | Baar Zug, Switzerland | Manufacturer | 1 | January 25, 2012 | 0 | 0 | 0 | api.fda.gov |
| Baechler Feintech AG | Hoelstein Basel-Landschaft, 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.