OraSure gets EUA for Ebola 2.0 test
Analysis based on 8 articles · First reported Jul 21, 2026 · Last updated Jul 21, 2026
OraSure's EUA positions it to capture significant demand during a global health emergency, potentially boosting revenues. The stock may see positive sentiment as the company scales production of a critical diagnostic tool.
OraSure Technologies received Emergency Use Authorization (EUA) from the U.S. United States — Food and Drug Administration (FDA) for its second-generation OraQuick Ebola 2.0 Rapid Antigen Test. The test detects all four Ebola viruses causing human disease, including the Bundibugyo virus responsible for the current outbreak in Central Africa. The authorization comes during an Ebola epidemic centered in the Democratic Republic of the Congo with cases in Uganda, which has prompted the World Health Organization to declare a global public health emergency. OraSure is ramping up production to meet demand. The test was developed with support from the United States — Biomedical Advanced Research and Development Authority (BARDA).
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