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Data / Medical devices / Jenner Stain

Jenner Stain (KJX): 4 FDA-registered makers in 1 country

4 establishments in 1 country are registered with the FDA to make Jenner Stain (product code KJX, Class 1, 21 CFR 864.1850). 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 September 11, 1984, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
KJX
Device class
1
Regulation
864.1850
Medical specialty
Hematology

Makers by country

CountryMakers
United States4

Makers of Jenner Stain

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
ENG Scientific LLCNew Brunswick, NJ, United StatesManufacturer0000api.fda.gov
Ethos Biosciences, INC.Logan Township, NJ, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Newcomer Supply IncWaunakee, WI, United StatesSpecification developer0000api.fda.gov
Richard-Allan Scientific LLCKalamazoo, MI, United StatesManufacturer0000api.fda.gov

Updated September 11, 1984. 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.