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Data / Medical devices / Reagents, Zika Virus Nucleic Acid

Reagents, Zika Virus Nucleic Acid (POA): 5 FDA-registered makers in 1 country

5 establishments in 1 country are registered with the FDA to make Reagents, Zika Virus Nucleic Acid (product code POA, Class N). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code
POA
Device class
N
Medical specialty
Unknown

Makers by country

CountryMakers
United States5

Makers of Reagents, Zika Virus Nucleic Acid

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
Abbott Molecular, Inc.Des Plaines, IL, United StatesManufacturer0000api.fda.gov
CodiagnosticsSalt Lake City, UT, United StatesManufacturer for export0000api.fda.gov
CTK Biotech, Inc.Poway, CA, United StatesManufacturer for export0000api.fda.gov
ELITechGroup MDX LLC.Bothell, WA, United StatesManufacturer0000api.fda.gov
Grifols Diagnostic Solutions Inc.San Diego, CA, United StatesContract 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.