Data / Medical devices / Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use / Switzerland
FDA-registered makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use in Switzerland: 6 establishments
6 establishments in Switzerland are registered with the FDA to make Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use (product code LXG). 0 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
- Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
- Product code
- LXG
- Country
- Switzerland
Makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Flex Precision Plastics Solutions (Switzerland) AG | Hagglingen Aargau, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Flex Precision Plastics Solutions AG | Kussnacht Schwyz, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nolato Treff AG | Degersheim Sankt Gallen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Roche Diagnostics International Ltd. | ROTKREUZ Zug, Switzerland | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weidmann Medical Technology AG | Rapperswil Sankt Gallen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weidmann Medical Technology AG | Bad Ragaz Sankt Gallen, 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.