Data / Medical devices / Oximeter / Switzerland
FDA-registered makers of Oximeter in Switzerland: 7 establishments
7 establishments in Switzerland are registered with the FDA to make Oximeter (product code DQA). 1 has 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
- Oximeter
- Product code
- DQA
- Country
- Switzerland
Makers of Oximeter in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Sentec AG | THERWIL Basel-Landschaft, Switzerland | Contract manufacturer, Manufacturer, Specification developer | 1 | September 12, 2007 | 0 | 0 | 0 | api.fda.gov |
| Corsano Health SA | Plan-les-Ouates Geneve, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hamilton Medical AG | BONADUZ Graubunden, Switzerland | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hamilton Medical AG | Domat / Ems Graubunden, Switzerland | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hamilton Medical AG | Domat/Ems Graubunden, Switzerland | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Radiometer Basel AG | BASEL Basel-Stadt, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Schiller AG | BAAR Zug, 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.