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Data / Medical devices / Device, General Purpose, Microbiology, Diagnostic / China

FDA-registered makers of Device, General Purpose, Microbiology, Diagnostic in China: 7 establishments

7 establishments in China are registered with the FDA to make Device, General Purpose, Microbiology, Diagnostic (product code LIB). 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
Device, General Purpose, Microbiology, Diagnostic
Product code
LIB
Country
China

Makers of Device, General Purpose, Microbiology, Diagnostic in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Boen Healthcare Co., Ltd.Suzhou Jiangsu, ChinaExporter to the US, Specification developer0000api.fda.gov
Changzhou DSB Medical Co., LtdChangzhou City Jiangsu, ChinaContract manufacturer0000api.fda.gov
Diatrust Medical Co., Ltd.Nanjing City Jiangsu, ChinaManufacturer0000api.fda.gov
Huzhou Junda Industry Co., Ltd.Anji Zhejiang, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Rusun Medical Co., LtdYichun City Jiangxi, ChinaManufacturer0000api.fda.gov
Xian Tianlong Science And Technology Co., Ltd.Xi'an Shaanxi, ChinaManufacturer0000api.fda.gov
Zhejiang Runlab Technology Co., Ltd.Taizhou 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.