Data / Medical devices / Frame, Spectacle / Austria
FDA-registered makers of Frame, Spectacle in Austria: 6 establishments
6 establishments in Austria are registered with the FDA to make Frame, Spectacle (product code HQZ). 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
- Frame, Spectacle
- Product code
- HQZ
- Country
- Austria
Makers of Frame, Spectacle in Austria
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Silhouette International Schmied AG | Linz Oberosterreich, Austria | Manufacturer | 1 | September 28, 1994 | 0 | 0 | 0 | api.fda.gov |
| Andy Wolf Fashion GMBH | Hartberg Steiermark, Austria | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eyewear Solution S GMBH | Hartberg Steiermark, Austria | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MPG Group GmbH | Graz Steiermark, Austria | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pomberger Goisern GMBH | Bad Goisern Oberosterreich, Austria | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| rolf.produktions GmbH | Weissenbach Tirol, Austria | 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.