Skip to the page

Data / Medical devices / Lens, Prescription, Color Deficiency

Lens, Prescription, Color Deficiency (NAI): 14 FDA-registered makers in 4 countries

14 establishments in 4 countries are registered with the FDA to make Lens, Prescription, Color Deficiency (product code NAI, Class 1, 21 CFR 886.5844). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on November 18, 1999, and lists 1 recall event (0 Class I). 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.

Product code
NAI
Device class
1
Regulation
886.5844
Medical specialty
Ophthalmic

Makers by country

CountryMakers
China5
United States5
Taiwan3
Spain1

Makers of Lens, Prescription, Color Deficiency

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Danyang Rimesis Optical Glasses Co.,ltdDanyang Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Enchroma, Inc.Berkeley, CA, United StatesSpecification developer0010api.fda.gov
Eyepol Optical Technology (xiamen) Co., Ltd.Xiamen Fujian, ChinaManufacturer0000api.fda.gov
IRENE CorporationTainan, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
JH Optical Co., Ltd.Tainan City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Shih Min Glasses Co., Ltd.Tainan City, TaiwanContract manufacturer0000api.fda.gov
Tecnologia Sostenible Y Responsable S.L.Madrid Madrid(Autonomous Community), SpainManufacturer0000api.fda.gov
Tsingtao Relly Optics Co., LtdQingdao Shandong, ChinaContract manufacturer, Exporter to the US, Manufacturer, Remanufacturer0000api.fda.gov
Vision Dynamics, LLCJeffersontown, KY, United StatesRemanufacturer0000api.fda.gov
Wal-Mart Optical LabFayetteville, AR, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Wal-Mart Optical Lab #9065Crawfordsville, IN, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Walmart Optical LabDallas, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Xiamen JS Polarizers Technology Co., Ltd.Xiamen City Fujian, ChinaExporter to the US, Manufacturer0000api.fda.gov
Zhejiang Sunny Optics Co.,Ltd.Yuyao City Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov

Updated November 18, 1999. 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.