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Data / Medical devices / Exerciser, Finger, Powered / China

FDA-registered makers of Exerciser, Finger, Powered in China: 8 establishments

8 establishments in China are registered with the FDA to make Exerciser, Finger, Powered (product code JFA). 0 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
Exerciser, Finger, Powered
Product code
JFA
Country
China

Makers of Exerciser, Finger, Powered in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Foshan Hongfeng Co.,ltdFoshan Guangdong, ChinaManufacturer0000api.fda.gov
Gizmospring.com Dongguan LimitedDongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Ningbo Dericsson Smart Technology Co.,ltd.Ningbo City Zhejiang, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Shenzhen Sungpo Hi-Tech Electronic Co., LtdShenzhen Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Shenzhen Willcareyou Technology Co., LtdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen XFT Medical LimitedShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Tuper Medical Co., Ltd.Dezhou City Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Zhejiang Todo Hardware Manufacture Co.,ltdJinhua Zhejiang, ChinaContract manufacturer, Manufacturer0000api.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.