Data / Medical devices / Frame, Spectacle / Denmark
FDA-registered makers of Frame, Spectacle in Denmark: 6 establishments
6 establishments in Denmark are registered with the FDA to make Frame, Spectacle (product code HQZ). 0 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
- Frame, Spectacle
- Product code
- HQZ
- Country
- Denmark
Makers of Frame, Spectacle in Denmark
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bellinger A/S | RISSKOV Midtjylland, Denmark | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Design Eyewear Group International A/S | Tranbjerg Midtjylland, Denmark | Exporter to the US, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fleye Aps | Hedehusene Hovedstaden, Denmark | Exporter to the US, Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lindberg A/S | AABYHOJ Midtjylland, Denmark | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Monoqool | Fredensborg Sjaelland, Denmark | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Skans Aps | Copenhagen Hovedstaden, Denmark | 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.