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Data / Medical devices / Lens, Spectacle, Non-Custom (Prescription) / Hong Kong

FDA-registered makers of Lens, Spectacle, Non-Custom (Prescription) in Hong Kong: 15 establishments

15 establishments in Hong Kong 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 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Lens, Spectacle, Non-Custom (Prescription)
Product code
HQG
Country
Hong Kong

Makers of Lens, Spectacle, Non-Custom (Prescription) in Hong Kong

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Argus Vision Intl. Ltd.Wan Chai, Hong Kong, Hong KongComplaint file establishment, Contract manufacturer, Contract sterilizer, Exporter to the US, Foreign private label distributor, Manufacturer, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer0000api.fda.gov
Arts Optical Company LimitedKowloon, Hong KongManufacturer0000api.fda.gov
Dragon Eyes Hong Kong LimitedCheung Sha Wan, Kowloon, Hong KongExporter to the US, Manufacturer0000api.fda.gov
H.K. Chaoxin Optical Co. Ltd.Tsuen Wan, Hong KongExporter to the US, Manufacturer0000api.fda.gov
Hong Kong Optical Lens Co., Ltd.Kwun Tong, Kowloon, Hong KongExporter to the US, Manufacturer, Specification developer0000api.fda.gov
Kelfred Optical Ltd.Shatin, N.T., Hong KongExporter to the US, Manufacturer0000api.fda.gov
Lancer Optical LimitedTsuen Wan, New Territories, Hong KongExporter to the US, Manufacturer0000api.fda.gov
Mazen Group LimitedHunghom, Kowloon, Hong KongExporter to the US, Manufacturer0000api.fda.gov
Okia Optical Co., Ltd.Kowloon, Hong KongExporter to the US, Manufacturer, Repackager or relabeler0000api.fda.gov
Premier Optical Mfy. Ltd.Kowloon Bay, Hong KongManufacturer0000api.fda.gov
Stepper Eyewear LimitedKowloon, Hong KongManufacturer0000api.fda.gov
Uf Accessories Co., LimitedSheung Wan, Hong KongExporter to the US, Manufacturer0000api.fda.gov
United Creation Optical Co.,ltdKowloon Bay, Kowloon, Hong KongExporter to the US, Manufacturer0000api.fda.gov
Win-Win Optics Co., LimitedHong Kong, Hong KongExporter to the US, Manufacturer0000api.fda.gov
World Dentists Association America LimitedTsim Sha, Hong KongManufacturer0000api.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.