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 ...
Antigen-detecting rapid diagnostic tests (Ag-RDTs) play a significant role in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing. Most Ag-RDTs currently used require nasopharyngeal ...
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 ...
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 ...
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, ...