SANTA CLARA, Calif., Oct. 21, 2021 /PRNewswire/ -- Xtrava Health, a health technology company, today announced the U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization ...
SUWON, South Korea--(BUSINESS WIRE)--SD Biosensor, Inc., a global in-vitro diagnostics company, is voluntarily recalling its STANDARD Q COVID-19 Ag Home Test in the United States, due to confirmed ...
Results are provided within 15 minutes and can be read directly from the testing card. The Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for BinaxNOW™ COVID-19 Ag ...
The World Health Organization (WHO) said on December 24, 2025, that it has prequalified two rapid antigen diagnostic tests (Ag-RDTs) for SARS-CoV-2, the virus that causes COVID-19. According to WHO, ...
In a recent study published on the preprint server medRxiv*, researchers analyze commercially available rapid antigen tests to evaluate their analytical sensitivity and specificity, as well as ...
JURUPA VALLEY, Calif.--(BUSINESS WIRE)--GenBody America, LLC, the U.S. affiliate of GenBody, Inc., a South Korean manufacturer of rapid diagnostic tests and reagents for point-of-care applications for ...
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