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Data / Medical devices / Chromatography (Liquid, Gel), Clinical Use

Chromatography (Liquid, Gel), Clinical Use (KZR): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Chromatography (Liquid, Gel), Clinical Use (product code KZR, Class 1, 21 CFR 862.2260). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 15 510(k) clearances under this code, the latest on October 6, 1997, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
KZR
Device class
1
Regulation
862.2260
Medical specialty
Clinical Chemistry

Makers by country

CountryMakers
China2
United States1

Makers of Chromatography (Liquid, Gel), Clinical Use

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Guang Xi Fulaiming Biopharmaceutics Co., Ltd.Nanning Guangxi, ChinaManufacturer0000api.fda.gov
Jiangsu Hongsheng Bioengineering Co., Ltd.Nantong Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
STS CorporationDuluth, GA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov

Updated October 6, 1997. 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.