Skip to the page

Data / Medical devices / Stimulator, Nerve, Transcutaneous, For Pain Relief / China

FDA-registered makers of Stimulator, Nerve, Transcutaneous, For Pain Relief in China: 28 establishments

28 establishments in China are registered with the FDA to make Stimulator, Nerve, Transcutaneous, For Pain Relief (product code GZJ). 10 have a 510(k) clearance or PMA approval on file and 0 have a recall event. 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.

Device
Stimulator, Nerve, Transcutaneous, For Pain Relief
Product code
GZJ
Country
China

Makers of Stimulator, Nerve, Transcutaneous, For Pain Relief in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Fuji Dynamics LimitedDongguan Guangdong, ChinaManufacturer5January 22, 2016000api.fda.gov
Wuxi Jiajian Medical Instrument Co., LtdWuxi Jiangsu, ChinaExporter to the US, Manufacturer4January 24, 2023000api.fda.gov
Bio Protech Yantai IncYantai Shandong, ChinaManufacturer2January 6, 2009000api.fda.gov
Easymed Instruments Co., Ltd.Daliang, Shunde, Foshan Guangdong, ChinaContract manufacturer, Manufacturer2June 5, 2012000api.fda.gov
Wat Medical Technology Inc.Ningbo Zhejiang, ChinaManufacturer2April 23, 2022000api.fda.gov
Bozhou Rongjian Medical Appliance Co., Ltd.Bozhou Anhui, ChinaExporter to the US, Manufacturer1May 25, 2022000api.fda.gov
Dongguan Bohuikang Technology Co.,ltdDongguan Guangdong, ChinaManufacturer1May 6, 1991000api.fda.gov
Dongguan Tutamen Metalwork Co.,LTD.Dongguan Guangdong, ChinaExporter to the US, Manufacturer1November 9, 2020000api.fda.gov
Netop Industrial Company LimitedDongguan Guangdong, ChinaManufacturer1April 19, 2024000api.fda.gov
Shenzhen Hengbosi Industrial Co., Ltd.Shenzhen Guangdong, ChinaManufacturer1June 17, 2003000api.fda.gov
ATL Technology DG,Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Chongqing Rob Linka Science And Technology Co., Ltd.Chongqing, ChinaExporter to the US, Manufacturer0000api.fda.gov
Edan Instruments, Inc.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Famidoc Technology Co., LtdDong Guan Guangdong, ChinaManufacturer0000api.fda.gov
Guangzhou Xinbo Electronic Co., Ltdguangzhou Guangdong, ChinaManufacturer0000api.fda.gov
Hebei Tuosite Technology Co.,ltdShijiazhuang Hebei, ChinaManufacturer0000api.fda.gov
Hong Qiangxing (shen Zhen) Electronics LimitedShenzhen Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Hang Yik Electronics Plastics & Mold (ShenZhen) Co., Ltd.Shenzhen Guangdong, ChinaContract manufacturer0000api.fda.gov
JKH Health Co., Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Shenzhen Kentro Medical Electronics Co., LtdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen Roundwhale Technology Co. Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen Willcareyou Technology Co., LtdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen XFT Medical LimitedShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen Zifound Infonet Technology Co., Ltd.SHENZHEN, GUANDONG Guangdong, ChinaContract manufacturer0000api.fda.gov
Shenzhen Dongdixin Technology Co., Ltd.SHENZHEN Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen Jie Zhong Lian Technology Co., Ltd.Shenzhen Guangdong, ChinaContract manufacturer0000api.fda.gov
Shenzhen OSTO Medical Technology Company LimitedShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Xemis Medical Technology (shenzhen) 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.