FDA 510(k) cleared point-of-care antigen test for rapid detection of SARS-CoV-2. Provides quick on-site diagnostic results for COVID-19 screening and confirmation.
Manufactured by
United States
Since 1996, InBios has been a leader in the development of diagnostic tests for emerging infectious diseases and biothreats. Products are designed for superior performance, efficiency and value. These include many FDA market authorized and CE marked assays for arboviruses, parasitic infections, biothreats, and more. InBios continues to anticipate and serve the growing global public health demand. Products in the pipeline include next generation platforms for tick-borne and respiratory diseases.
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