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Data / Medical devices / Sunglasses (Non-Prescription Including Photosensitive) / Cambodia

FDA-registered makers of Sunglasses (Non-Prescription Including Photosensitive) in Cambodia: 5 establishments

5 establishments in Cambodia 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.

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
Sunglasses (Non-Prescription Including Photosensitive)
Product code
HQY
Country
Cambodia

Makers of Sunglasses (Non-Prescription Including Photosensitive) in Cambodia

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Bestfine (Cambodia) Swimming Appliances Co., Ltd.Kong Pisei District Kampong Speu, CambodiaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Cam-Icare Co., Ltd.Sihanoukville Preah Sihanouk, CambodiaExporter to the US, Manufacturer0000api.fda.gov
Hongfu Optical (cambodia) Co., LtdTRIENG DISTRICT Takeo, CambodiaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
United Creation Optical (Cambodia) Co., Ltd.Samraong Tong District Kampong Speu, CambodiaExporter to the US, Manufacturer0000api.fda.gov
Vision 26 Optical Manufacturing (cambodia) LimitedSiem Reap Province, CambodiaManufacturer0000api.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.