(RTTNews) - LumiraDx Ltd. (LMDX), a diagnostics company, announced Friday that its rapid COVID-19 antigen assay, LumiraDx SARS-CoV-2 Ag Test has successfully received the Emergency Use Listing or EUL ...
In a recent retrospective cross-sectional study posted to The Lancet* preprint server, researchers assessed rapid antigen (Ag) tests for identifying severe acute respiratory syndrome coronavirus-2 ...
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 ...
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