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Data / Medical devices / Labware, Assisted Reproduction / China

FDA-registered makers of Labware, Assisted Reproduction in China: 7 establishments

7 establishments in China are registered with the FDA to make Labware, Assisted Reproduction (product code MQK). 2 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
Labware, Assisted Reproduction
Product code
MQK
Country
China

Makers of Labware, Assisted Reproduction in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Gimbo Medical Technology Shenzhen Co., Ltd.Shenzhen Guangdong, ChinaManufacturer1June 14, 2024000api.fda.gov
Guangzhou Hehong Biotech Co., Ltd.Guangzhou Guangdong, ChinaManufacturer1February 3, 2025000api.fda.gov
Hua Yue Medical Technology Co., Ltd.Guangzhou Guangdong, ChinaManufacturer0000api.fda.gov
Shandong Wego Ruisheng Medical Device Co.,ltdWeihai Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shenzhen Boomingshing Medical Device Co., LtdShenzhen Guangdong, ChinaContract manufacturer0000api.fda.gov
Shenzhen VitaVitro Biotech Co.,Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Wuhan Huchuang Union Technology Co., Ltd.Wuhan Hubei, ChinaExporter 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.