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Data / Medical devices / Reagents, Ebola Zaire Virus (Detected In The West Africa Outbreak In 2014) Nucleic Acid / United States

FDA-registered makers of Reagents, Ebola Zaire Virus (Detected In The West Africa Outbreak In 2014) Nucleic Acid in the United States: 5 establishments

5 establishments in the United States are registered with the FDA to make Reagents, Ebola Zaire Virus (Detected In The West Africa Outbreak In 2014) Nucleic Acid (product code POG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. 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.

Device
Reagents, Ebola Zaire Virus (Detected In The West Africa Outbreak In 2014) Nucleic Acid
Product code
POG
Country
United States

Makers of Reagents, Ebola Zaire Virus (Detected In The West Africa Outbreak In 2014) Nucleic Acid in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
BioFire Defense, LLCSalt Lake City, UT, United StatesManufacturer0000api.fda.gov
Chembio Diagnostic Systems, Inc.Medford, NY, United StatesManufacturer for export0000api.fda.gov
Chembio Diagnostic SystemsBay Shore, NY, United StatesManufacturer for export0000api.fda.gov
Orasure Technologies, Inc.Bethlehem, PA, United StatesManufacturer0000api.fda.gov
Orasure Technologies, Inc.Bethlehem, PA, United StatesManufacturer0000api.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.