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Data / Medical devices / Goniometer, Nonpowered / China

FDA-registered makers of Goniometer, Nonpowered in China: 13 establishments

13 establishments in China are registered with the FDA to make Goniometer, Nonpowered (product code KQW). 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
Goniometer, Nonpowered
Product code
KQW
Country
China

Makers of Goniometer, Nonpowered in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Anji Hengfeng Sanitary Material Co., Ltd.Anji Zhejiang, ChinaManufacturer0000api.fda.gov
Guangzhou Goldsun Electronic Co. LtdGuangzhou Guangdong, ChinaContract 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
Hangzhou Tangda Technology Co., LtdHangzhou City Zhejiang, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
HANGZHOU TUOPUSI MEDICAL PRODUCTS Co. LtdHangzhou City Zhejiang, ChinaManufacturer0000api.fda.gov
Ningbo Castle Medical Import & Export Co.,ltdNingbo Zhejiang, ChinaContract manufacturer0000api.fda.gov
Ningbo Magic Time Medical Equipment Co.,ltd.NINGBO Zhejiang, ChinaContract manufacturer0000api.fda.gov
Ningbo Ningyuan Import & Export Co., Ltd.Ningbo, Zhejiang, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
Wenzhou Caretek Medical Device Co., LtdWenzhou Zhejiang, ChinaExporter to the US, Manufacturer0000api.fda.gov
Wenzhou Longwan Medical Device FactoryWenzhou Zhejiang, ChinaManufacturer0000api.fda.gov
Xinhua Healthcare Industry Co.,limitedZibo Shandong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Zhejiang Econns Industry Co., LimitedJinhua City Zhejiang, ChinaContract manufacturer, Exporter to the US, 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.