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Data / Medical devices / Plasmodium Spp. Detection Reagents / United States

FDA-registered makers of Plasmodium Spp. Detection Reagents in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Plasmodium Spp. Detection Reagents (product code OAX). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Plasmodium Spp. Detection Reagents
Product code
OAX
Country
United States

Makers of Plasmodium Spp. Detection Reagents in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abbott Diagnostics Scarborough, Inc.Scarborough, ME, United StatesManufacturer1June 13, 2007000api.fda.gov
Abbott Diagnostics Scarborough, Inc.Westbrook, ME, United StatesManufacturer1June 13, 2007000api.fda.gov
Access Bio, Inc.Monroe Township, NJ, United StatesManufacturer for export0000api.fda.gov
Boston Easy Biotech IncBelmont, MA, United StatesManufacturer for export0000api.fda.gov
CTK Biotech, Inc.Poway, CA, United StatesManufacturer for export0000api.fda.gov
Premier Medical Usa CorporationSomerset, NJ, United StatesManufacturer for export0000api.fda.gov
Trinity Biotech USAJamestown, NY, United StatesManufacturer for export0000api.fda.gov

Updated November 3, 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.