Data / Medical devices / Sunglasses (Non-Prescription Including Photosensitive) / Canada
FDA-registered makers of Sunglasses (Non-Prescription Including Photosensitive) in Canada: 10 establishments
10 establishments in Canada 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 2, 2026.
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- Device
- Sunglasses (Non-Prescription Including Photosensitive)
- Product code
- HQY
- Country
- Canada
Makers of Sunglasses (Non-Prescription Including Photosensitive) in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| 1266881 B.C. | Coquitlam British Columbia, Canada | Exporter to the US, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ardene International Inc. | Montreal Quebec, Canada | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Faniel Inc. | Val-Morin Quebec, Canada | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kits Eyecare Ltd | VANCOUVER British Columbia, Canada | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lunetterie Generale Inc | Repentigny Quebec, Canada | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Optiques Sher-Lab Inc | Sherbrooke Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Safilo Canada, Inc. | Montreal Quebec, Canada | Repackager or relabeler, Reprocessor | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spectacle Eyeworks Inc. | North Vancouver British Columbia, Canada | Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Welcome Studios Ltd. | Vancouver British Columbia, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| WestGroupe Optical Inc. | Ville St-Laurent Quebec, Canada | Exporter to the US, Specification developer | 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.