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Data / Medical devices / Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) / Vietnam

FDA-registered makers of Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) in Vietnam: 10 establishments

10 establishments in Vietnam are registered with the FDA to make Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) (product code HOY). 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
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
Product code
HOY
Country
Vietnam

Makers of Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) in Vietnam

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
An Lanh Investment And Trading Company LimitedThanh Nam Ward Ninh Binh, VietnamContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Creation Optical Vietnam Co.,ltdBac Ninh, VietnamExporter to the US, Manufacturer0000api.fda.gov
Dang Phi Industrial And Trading Company LimitedYen Phong District Bac Ninh, VietnamExporter to the US, Manufacturer0000api.fda.gov
Hindar Optical Viet Nam Company LimitedBac Ninh, VietnamContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Lancer Optical (vietnam) Company LimitedXuan Cam Commune Bac Ninh, VietnamExporter to the US, Manufacturer0000api.fda.gov
Nhan Duc Industrial Co., LtdDong Nai, VietnamManufacturer0000api.fda.gov
Okia Vietnam Optical Co Ltd.Tay Ninh, VietnamManufacturer0000api.fda.gov
Topway Sports Enterprise Co LtdTAN UYEN TOWN Binh Duong, VietnamManufacturer0000api.fda.gov
Union Eyewear Vietnam Company LimitedViet Tien Commune Hung Yen, VietnamExporter to the US, Manufacturer0000api.fda.gov
Vietnam Aishi Optics Company LimitedLang Giang District Bac Ninh, VietnamContract manufacturer, Manufacturer0000api.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.