Data / Medical devices / Sunglasses (Non-Prescription Including Photosensitive) / Spain
FDA-registered makers of Sunglasses (Non-Prescription Including Photosensitive) in Spain: 8 establishments
8 establishments in Spain are registered with the FDA to make Sunglasses (Non-Prescription Including Photosensitive) (product code HQY). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Sunglasses (Non-Prescription Including Photosensitive)
- Product code
- HQY
- Country
- Spain
Makers of Sunglasses (Non-Prescription Including Photosensitive) in Spain
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| D & R Optical S.L. | Bellaterra Barcelona, Spain | Exporter to the US, Foreign private label distributor, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kaleos Eyehunters SL | Barcelona, Spain | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Maison Nina, SL | Madrid Madrid(Autonomous Community), Spain | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Offview SL | Cerdanyola del Valles Barcelona, Spain | Exporter to the US, Foreign private label distributor, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Play Hawkers S.L. | Elche Alicante, Spain | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solo Gafas S.L. | Barcelona, Spain | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tecnologia Sostenible Y Responsable S.L. | Madrid Madrid(Autonomous Community), Spain | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tressol S.A. | ESPLUGUES DE LLOBREGAT Barcelona, Spain | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.