Data / Medical devices / Frame, Spectacle / Germany
FDA-registered makers of Frame, Spectacle in Germany: 19 establishments
19 establishments in Germany 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
- Germany
Makers of Frame, Spectacle in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| LUNOR Aktiengesellschaft | Bad Liebenzell Baden-Wurttemberg, Germany | Contract manufacturer, Manufacturer | 1 | December 8, 1993 | 0 | 0 | 0 | api.fda.gov |
| A. Schweizer GMBH | FORCHHEIM Bavaria, Germany | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Additive Scale GMBH | Krailling Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carl Zeiss Vision GMBH | AALEN Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DR. EUGEN BECK GmbH & Co. FLAIR | Passau Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fielmann Group AG | Hamburg, Germany | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ivko GMBH | NITZ Rhineland-Palatinate, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lotos Goldbrillen GMBH | Eisingen Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Maybach Icons Of Luxury GMBH | Baar Rhineland-Palatinate, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mykita GMBH | berlin, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Op Couture Brillen GMBH | PASSAU Bavaria, Germany | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| OWP Brillen GmbH | Passau Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PM Frost GMBH - Eyewear & Accessories | SASBACH Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rodenstock GmbH | Munich Bavaria, Germany | Foreign private label distributor, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Schnuchel | Holm Schleswig-Holstein, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Walter Wissing & Co. Inh. Olaf Lauer | Bensheim Hesse, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weareannu GMBH | Nuremberg Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zettner Brillenfabrikation GMBH | Furth Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ic! berlin GmbH | Berlin, Germany | 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.