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Data / Medical devices / Hysteroscope Accessories / China

FDA-registered makers of Hysteroscope Accessories in China: 12 establishments

12 establishments in China are registered with the FDA to make Hysteroscope Accessories (product code NWW). 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
Hysteroscope Accessories
Product code
NWW
Country
China

Makers of Hysteroscope Accessories in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Anhui Shiyin Photoelectric Instrument Co., Ltd.Suzhou Anhui, ChinaManufacturer, Specification developer0000api.fda.gov
Guangzhou Red Pine Medical Instrument Co.,ltd.Guangzhou Guangdong, ChinaManufacturer0000api.fda.gov
Guangdong MacroLux Medical Technology Co., Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Hangzhou Fushan Medical Appliance Co., Ltd.Hangzhou City Zhejiang, ChinaContract manufacturer, Contract sterilizer0000api.fda.gov
Jiangsu Jiyuan Medical Technology Co., Ltd.Taizhou Jiangsu, ChinaComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Macrolux Medical Technology Co., Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Origyn Medical Technology (hangzhou) Co., LtdHangzhou Zhejiang, ChinaManufacturer, Specification developer0000api.fda.gov
Suzhou Acuvu Medical Technology Co., Ltd.Suzhou Jiangsu, ChinaSpecification developer0000api.fda.gov
Tonglu Wanhe Medical Instrument Co., Ltd.Hangzhou Zhejiang, ChinaExporter to the US, Manufacturer0000api.fda.gov
Xuzhou AKX Electronic Science and Technology Co., Ltd.Xuzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Zhejiang Chuangxiang Medical Technology Co., Ltd.Hangzhou Zhejiang, ChinaManufacturer0000api.fda.gov
Zhuji Pengtian Medical Instrument Co.,Ltd.Zhuji Zhejiang, ChinaManufacturer0000api.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.