Skip to the page

Data / Medical devices / Stains, Microbiologic

Stains, Microbiologic (JTS): 29 FDA-registered makers in 6 countries

29 establishments in 6 countries are registered with the FDA to make Stains, Microbiologic (product code JTS, Class 1, 21 CFR 864.1850). 2 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 40 510(k) clearances under this code, the latest on March 19, 1996, and lists 6 recall events (0 Class I). FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Product code
JTS
Device class
1
Regulation
864.1850
Medical specialty
Hematology

Makers by country

CountryMakers
United States22
Germany2
France2
Canada1
South Korea1
Mexico1

Makers of Stains, Microbiologic

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
Remel, Inc.Lenexa, KS, United StatesManufacturer, Specification developer8March 19, 1996010api.fda.gov
CalibreScientific US, Inc.Vancouver, WA, United StatesManufacturer2May 13, 1988000api.fda.gov
Azer Scientific, Inc.Morgantown, PA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Becton, Dickinson & Co.Sparks, MD, United StatesManufacturer0040api.fda.gov
Bio-Gram Diagnostics GMBHWorms Rhineland-Palatinate, GermanyManufacturer0000api.fda.gov
Biogenex Laboratories Inc.Fremont, CA, United StatesManufacturer0000api.fda.gov
Biomerieux SALA BALME LES GROTTES Isere, FranceManufacturer, Specification developer0000api.fda.gov
Biomerieux, Inc.Hazelwood, MO, United StatesManufacturer, Specification developer0000api.fda.gov
Chaptec AmericaMontreal Quebec, CanadaManufacturer0000api.fda.gov
Dagatronics CorporationGoyang Gyeonggi, South KoreaManufacturer0000api.fda.gov
E K Industries, Inc.Joliet, IL, United StatesManufacturer0000api.fda.gov
ELITechGroup IncLogan, UT, United StatesManufacturer0000api.fda.gov
Emd Millipore CorporationBurlington, MA, United StatesSpecification developer0000api.fda.gov
Ethos Biosciences, INC.Logan Township, NJ, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Hardy DiagnosticsOrcutt, CA, United StatesManufacturer0000api.fda.gov
James Alexander Corp.Blairstown, NJ, United StatesContract manufacturer0000api.fda.gov
Medical Chemical CorporationTorrance, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Merck KgaaDARMSTADT Hesse, GermanyManufacturer0000api.fda.gov
Meridian Bioscience, Inc.Cincinnati, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Microbiologics, Inc.Saint Cloud, MN, United StatesManufacturer0000api.fda.gov
Newcomer Supply IncWaunakee, WI, United StatesSpecification developer0000api.fda.gov
Polysciences, Inc.Warrington, PA, United StatesManufacturer0000api.fda.gov
Ral DiagnosticsMartillac Gironde, FranceManufacturer0000api.fda.gov
Richard-Allan Scientific LLCKalamazoo, MI, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Rocky Mountain Reagents, Inc.Golden, CO, United StatesManufacturer0000api.fda.gov
RR Donnelley Global Turnkey SolutionsJuarez Chihuahua, MexicoContract manufacturer, Repackager or relabeler0000api.fda.gov
Teco DiagnosticsAnaheim, CA, United StatesManufacturer0000api.fda.gov
Ventana Medical Systems, Inc.Tucson, AZ, United StatesManufacturer0000api.fda.gov
VolusolTooele, UT, United StatesManufacturer0000api.fda.gov

Updated March 19, 1996. 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.