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Data / Medical devices / Densitometeric, Protein Fractionation

Densitometeric, Protein Fractionation (JQJ): 3 FDA-registered makers in 3 countries

3 establishments in 3 countries are registered with the FDA to make Densitometeric, Protein Fractionation (product code JQJ, Class 1, 21 CFR 862.1630). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on June 12, 1990, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
JQJ
Device class
1
Regulation
862.1630
Medical specialty
Clinical Chemistry

Makers by country

CountryMakers
United States1
France1
China1

Makers of Densitometeric, Protein Fractionation

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
Helena Laboratories, Corp.Beaumont, TX, United StatesManufacturer0000api.fda.gov
SebiaEVRY Essonne, FranceManufacturer0000api.fda.gov
Zhejiang Orient Gene BiotechHuzhou Zhejiang, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov

Updated June 12, 1990. 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.