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Data / Medical devices / Lens, Spectacle (Prescription), For Reading Discomfort / Taiwan

FDA-registered makers of Lens, Spectacle (Prescription), For Reading Discomfort in Taiwan: 13 establishments

13 establishments in Taiwan are registered with the FDA to make Lens, Spectacle (Prescription), For Reading Discomfort (product code NJH). 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 (Prescription), For Reading Discomfort
Product code
NJH
Country
Taiwan

Makers of Lens, Spectacle (Prescription), For Reading Discomfort in Taiwan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Argus Vision Intl. Ltd.Tainan, TaiwanManufacturer0000api.fda.gov
Aswan International CorporationTaipei, TaiwanContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Aurora Optic Inc.CHIAYI Chiayi(County), TaiwanManufacturer0000api.fda.gov
Cji Ltd.Tainan, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
Day Sun Technology LimitedTainan, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
ESSILORLUXOTTICA ASIA PACIFIC PTE LTD. TGT Taiwan Branch (SINGAPORE)Tainan, TaiwanContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
First Rank Co., LtdNew Taipei, TaiwanManufacturer0000api.fda.gov
IRENE CorporationTainan, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
Jiann Lih Optical Co., Ltd.TAINAN City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
JP Optical Pte Ltd.Tainan City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Sunever Eyewear Co., Ltd.Tainan City, TaiwanManufacturer0000api.fda.gov
Tsair Yuarn Industrial Co., Ltd.Tainan City, TaiwanManufacturer0000api.fda.gov
Well Sun Optical Technology Limited.Tainan, TaiwanManufacturer0000api.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.