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Data / Medical devices / Slide Stainer, Automated / China

FDA-registered makers of Slide Stainer, Automated in China: 14 establishments

14 establishments in China are registered with the FDA to make Slide Stainer, Automated (product code KPA). 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
Slide Stainer, Automated
Product code
KPA
Country
China

Makers of Slide Stainer, Automated in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ave Science & Technology Co., LtdChangsha Hunan, ChinaExporter to the US, Manufacturer0000api.fda.gov
Dakewe(shenzhen) Medical Equipment Co., LtdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Diatrust Medical Co., Ltd.Nanjing City Jiangsu, ChinaManufacturer0000api.fda.gov
Fuzhou Maixin Biotech Co., Ltd.Fuzhou City Fujian, ChinaManufacturer0000api.fda.gov
Hangzhou Healthsky Biotechnology Co., Ltd.Hangzhou City Zhejiang, ChinaManufacturer0000api.fda.gov
Henan Celnovte Biotechnology Co., Ltd.zhengzhou Henan, ChinaManufacturer0000api.fda.gov
Infitek Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Jiangsu Medomics Medical Technology Co., Ltd.Nanjing Jiangsu, ChinaManufacturer0000api.fda.gov
Labpeak Co.,ltdJinan Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Leica Instruments (Shanghai) Co., Ltd.Shanghai, ChinaSpecification developer0000api.fda.gov
Scitek Global Co.,ltdJinan Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shenzhen Dartmon Biotechnology Co., Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Wuhan Landing Intelligence Medical Co.,LtdWuhan Hubei, ChinaManufacturer0000api.fda.gov
Zhejiang Gene Science Co., Ltdshaoxing Zhejiang, 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.