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Data / Medical devices / Hematoxylin Harris'S

Hematoxylin Harris'S (HYK): 24 FDA-registered makers in 4 countries

24 establishments in 4 countries are registered with the FDA to make Hematoxylin Harris'S (product code HYK, 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 7 510(k) clearances under this code, the latest on August 21, 1987, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
HYK
Device class
1
Regulation
864.1850
Medical specialty
Hematology

Makers by country

CountryMakers
United States20
China2
Canada1
Germany1

Makers of Hematoxylin Harris'S

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
ANATECH division of Cancer Diagnostics, Inc.Battle Creek, MI, United StatesManufacturer0000api.fda.gov
Azer Scientific, Inc.Morgantown, PA, United StatesComplaint file establishment, Contract manufacturer, Manufacturer0000api.fda.gov
Chaptec AmericaMontreal Quebec, CanadaManufacturer0000api.fda.gov
CITOTEST Labware Manufacturing CO., LTD.Haimen Jiangsu, ChinaManufacturer0000api.fda.gov
Citotest Scientific Co.,ltd.Nanjing Jiangsu, ChinaManufacturer, Repackager or relabeler0000api.fda.gov
Cancer Diagnostics, Inc.Durham, NC, United StatesManufacturer0000api.fda.gov
Delasco, LLCPlano, TX, United StatesManufacturer0000api.fda.gov
E K Industries, Inc.Joliet, IL, United StatesManufacturer0000api.fda.gov
Emd Millipore CorporationBurlington, MA, United StatesSpecification developer0000api.fda.gov
ENG Scientific LLCNew Brunswick, NJ, United StatesManufacturer0000api.fda.gov
Ethos Biosciences, INC.Logan Township, NJ, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Leica Biosystems Richmond, Inc.Richmond, IL, United StatesManufacturer0000api.fda.gov
Medical Chemical CorporationTorrance, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Merck KgaaDARMSTADT Hesse, GermanyManufacturer0000api.fda.gov
Newcomer Supply IncWaunakee, WI, United StatesSpecification developer0000api.fda.gov
Polysciences, Inc.Warrington, PA, United StatesManufacturer0000api.fda.gov
Ricca Chemical Company LLCPocomoke City, MD, United StatesManufacturer0000api.fda.gov
Ricca Chemical Company LLCArlington, TX, United StatesManufacturer0000api.fda.gov
Ricca Chemical Company LLCBatesville, IN, United StatesManufacturer0000api.fda.gov
Richard-Allan Scientific LLCKalamazoo, MI, United StatesManufacturer0000api.fda.gov
Scytek Laboratories, Inc.Logan, UT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Sigma-Aldrich Manufacturing, LLC-H&HSaint Louis, MO, United StatesManufacturer0000api.fda.gov
SLMP LLC d.b.a. StatLab Medical ProductsMcKinney, TX, United StatesContract manufacturer, Manufacturer0000api.fda.gov
SSN SolutionsHenrico, VA, United StatesManufacturer0000api.fda.gov

Updated August 21, 1987. 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.