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Data / Medical devices / Assembly, Tube Housing, X-Ray, Diagnostic / China

FDA-registered makers of Assembly, Tube Housing, X-Ray, Diagnostic in China: 13 establishments

13 establishments in China are registered with the FDA to make Assembly, Tube Housing, X-Ray, Diagnostic (product code ITY). 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
Assembly, Tube Housing, X-Ray, Diagnostic
Product code
ITY
Country
China

Makers of Assembly, Tube Housing, X-Ray, Diagnostic in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Beijing Smartbeam Medical Devices Co., LTDBeijing, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Ge Hangwei Medical Systems Co., Ltd.Beijing, ChinaManufacturer0000api.fda.gov
GE Healthcare (China) Co., Ltd.Beijing, ChinaSpecification developer0000api.fda.gov
Hangzhou Kailong Medical Instruments Co., Ltd.Hangzhou Zhejiang, ChinaManufacturer0000api.fda.gov
Konason (guangdong) Medical Imaging Technology Co., LtdDongguan Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Mingwei Medical Technology(suzhou) Co.,ltdSuzhou Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Micro X-ray Technology (Suzhou) Co., Ltdsuzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Siemens X-Ray Vacuum Technology Ltd.Wuxi Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Spellman High Voltage Electronics(suzhou Industrial Park)co.,ltdSuzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Varex Imaging Equipment (China) Co., LTDWuxi Jiangsu, ChinaContract manufacturer0000api.fda.gov
Wuxi Guochen Medical Technology Co., Ltd.Wuxi Jiangsu, ChinaManufacturer0000api.fda.gov
Wuxi Yushou Medical Appliances Co., LtdWuxi City Jiangsu, ChinaManufacturer0000api.fda.gov
Zhuhai Niray Photon Technology Co., Ltd.Zhuhai Guangdong, 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.