Data / Medical devices / Lens, Spectacle, Non-Custom (Prescription) / Canada
FDA-registered makers of Lens, Spectacle, Non-Custom (Prescription) in Canada: 9 establishments
9 establishments in Canada are registered with the FDA to make Lens, Spectacle, Non-Custom (Prescription) (product code HQG). 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
- Lens, Spectacle, Non-Custom (Prescription)
- Product code
- HQG
- Country
- Canada
Makers of Lens, Spectacle, Non-Custom (Prescription) 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 | |
| Centennial Optical Ltd. | Toronto Ontario, Canada | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Costco Wholesale Optical Lab 566 | Boisbriand Quebec, Canada | Manufacturer, Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carl Zeiss Vision Canada, Inc. | Toronto Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hoya Lens Canada, Inc. | Mississauga Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Newlook Vision Group Inc. | Montreal Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nikon Optical Canada, Inc. | Montreal Quebec, Canada | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shamir Canada | London Ontario, 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.