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Data / Medical devices / Microtools, Assisted Reproduction (Pipettes), Exempt / China

FDA-registered makers of Microtools, Assisted Reproduction (Pipettes), Exempt in China: 7 establishments

7 establishments in China are registered with the FDA to make Microtools, Assisted Reproduction (Pipettes), Exempt (product code PUC). 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
Microtools, Assisted Reproduction (Pipettes), Exempt
Product code
PUC
Country
China

Makers of Microtools, Assisted Reproduction (Pipettes), Exempt in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Arsci Biomedical Inc.Jiaxing Zhejiang, ChinaManufacturer0000api.fda.gov
Donnevie Medical Technology (shanghai) Co.ltdShanghai, ChinaManufacturer0000api.fda.gov
Guangzhou PINZHI Medical Device Co., Ltd.Guangzhou Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Jiangsu Kangjian Medical Apparatus Co., Ltd.JIANGYAN Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Shenzhen VitaVitro Biotech Co.,Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
UKS Medical Technology (Chongqing) Co., Ltd.Chongqing, ChinaManufacturer0000api.fda.gov
Wuhan Huchuang Union Technology Co., Ltd.Wuhan Hubei, 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.