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Data / Medical devices / Colorimeter, Photometer, Spectrophotometer For Clinical Use / China

FDA-registered makers of Colorimeter, Photometer, Spectrophotometer For Clinical Use in China: 12 establishments

12 establishments in China are registered with the FDA to make Colorimeter, Photometer, Spectrophotometer For Clinical Use (product code JJQ). 1 has 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
Colorimeter, Photometer, Spectrophotometer For Clinical Use
Product code
JJQ
Country
China

Makers of Colorimeter, Photometer, Spectrophotometer For Clinical Use in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Chong Qing Teco Huayi Pharm. Co.Shapingba Dist., Chongqing, ChinaContract manufacturer, Manufacturer, Repackager or relabeler2March 1, 1990000api.fda.gov
Biobase Biodustry(shandong)co., LtdJinan Shandong, ChinaManufacturer0000api.fda.gov
Dirui Industrial Co., Ltd.CHANGCHUN Jilin, ChinaManufacturer0000api.fda.gov
Genrui Biotech IncShenzhen Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Guangzhou Konmison Technology Co., Ltd.Guangzhou Guangdong, ChinaManufacturer0000api.fda.gov
Infitek Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Labpeak Co.,ltdJinan Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Scitek Global Co.,ltdJinan Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shanghai Kehua Laboratory System Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Shijiazhuang Hipro Biotechnology Co.,ltdShijiazhuang Hebei, ChinaManufacturer0000api.fda.gov
Unico (shanghai) Instrument Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Zhejiang Orient Gene BiotechHuzhou 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.