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Data / Medical devices / Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp. / United States

FDA-registered makers of Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp. in the United States: 6 establishments

6 establishments in the United States are registered with the FDA to make Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp. (product code KHW). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.
Product code
KHW
Country
United States

Makers of Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp. in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Techlab, Inc.Radford, VA, United StatesManufacturer2June 7, 2017000api.fda.gov
Techlab, Inc.Blacksburg, VA, United StatesManufacturer2June 7, 2017000api.fda.gov
Aceso Laboratories Inc.Chino, CA, United StatesManufacturer0000api.fda.gov
Eiger Diagnostics, Inc.Las Vegas, NV, United StatesSpecification developer0000api.fda.gov
Immunocentrix CorporationCanoga Park, CA, United StatesManufacturer for export0000api.fda.gov
New Life Diagnostics Inc.Carlsbad, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov

Updated November 2, 2026. 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.