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Data / Medical devices / Stirrup, External Brace Component / China

FDA-registered makers of Stirrup, External Brace Component in China: 6 establishments

6 establishments in China are registered with the FDA to make Stirrup, External Brace Component (product code ITC). 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
Stirrup, External Brace Component
Product code
ITC
Country
China

Makers of Stirrup, External Brace Component in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abletech Orthopedics CorporationNew Taipei City Taiwan, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
Dongguan SAVA Sporting Products Co.,LtdDongguan City Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Guangdong Hexin Technology Weaving Co., LTDHuizhou City Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
GuoLong (Shenzhen) High Technology Co., LtdShenzhen Guangdong, ChinaContract manufacturer0000api.fda.gov
Zhangpu Ortholife Rehabilitation Co., LtdZhangzhou Fujian, ChinaManufacturer0000api.fda.gov
Zhangzhou Recaring Medical Instrument Co., LtdZhangzhou Fujian, 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.