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Data / Medical devices / Led Light Source / China

FDA-registered makers of Led Light Source in China: 13 establishments

13 establishments in China are registered with the FDA to make Led Light Source (product code NTN). 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
Led Light Source
Product code
NTN
Country
China

Makers of Led Light Source in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Anqing Changfan Medical Instrument Co., LtdAnqing Anhui, ChinaExporter to the US, Manufacturer0000api.fda.gov
Dongguan Miqiang Technology Co., LtdDongguan Guangdong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Guangdong Optomedic Technologies, Inc.Foshan Guangdong, ChinaManufacturer0000api.fda.gov
Hunan Endoso Life Technology Co., LtdXiangTan Hunan, ChinaManufacturer0000api.fda.gov
Micro-Tech (Nanjing) Co., Ltd.Nanjing Jiangsu, ChinaManufacturer0000api.fda.gov
Micro-Tech (Nanjing) Co., Ltd.NAN JING Jiangsu, ChinaManufacturer0000api.fda.gov
Scivita Medical Technology Co., Ltd.suzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Shanghai Seegen Photoelectric Technology Co., LtdShanghai, ChinaManufacturer0000api.fda.gov
Shanghai Seegen Photoelectric Technology Co., LtdShanghai, ChinaManufacturer0000api.fda.gov
Shenzhen Eyco Technology Co.,ltdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen Hugemed Medical Technical Development Co., LtdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen Sophway Technology Co., Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen Yiguangnian Innovation Technology Co., Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.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.