Data / Medical devices / Spirometer, Diagnostic / Switzerland
FDA-registered makers of Spirometer, Diagnostic in Switzerland: 6 establishments
6 establishments in Switzerland are registered with the FDA to make Spirometer, Diagnostic (product code BZG). 3 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
- Spirometer, Diagnostic
- Product code
- BZG
- Country
- Switzerland
Makers of Spirometer, Diagnostic in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| NDD Medizintechnik AG | Zurich, Switzerland | Complaint file establishment, Manufacturer, Specification developer | 4 | October 19, 2023 | 0 | 0 | 0 | api.fda.gov |
| Pall International, Sarl | Fribourg, Switzerland | Exporter to the US, Specification developer | 1 | November 7, 1985 | 0 | 0 | 0 | api.fda.gov |
| Schiller AG | BAAR Zug, Switzerland | Manufacturer | 1 | April 30, 1999 | 0 | 0 | 0 | api.fda.gov |
| Corsano Health SA | Plan-les-Ouates Geneve, Switzerland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Variosystems AG | Steinach Sankt Gallen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zollner Electronics GMBH | Hombrechtikon Zurich, 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.