Portable COVID-19 Test Instrument Uses Bulk Acoustic Wave Technology to Achieve SARS-CoV-2 Antigen Testing in 20 Minutes

Food and Drug Administration (FDA) for its Qorvo Omnia SARS-CoV-2 Antigen Test. The test is authorized for the qualitative detection of nucleocapsid viral antigens from SARS-CoV-2 in nasal swab specimens from individuals who are suspected of COVID-19.

The Qorvo Omnia platform features a portable test instrument, microfluidic cartridge and secure connectivity. The microfluidic cartridge design enables specific binding with additional wash steps similar to central lab instrument operation and demonstrated results including 100% specificity during clinical trials. BAW sensor technology enables low Limit of Detection (LOD) levels that are similar to molecular testing capability.

“This is very exciting news. FDA authorization of Qorvo’s Omnia Antigen Test provides a rapid, sensitive and specific assessment of individuals, assisting providers trying to either rule in or rule out COVID-19, comparable to many of the PCR testing platforms in use,” said Fred S. Apple, Ph.D., a member of Qorvo Biotechnologies’ advisory board, Co-Medical Director of Toxicology Laboratory at Hennepin Healthcare/Hennepin County Medical Center, and Professor of Laboratory Medicine & Pathology at the University of Minnesota. “The testing system will hopefully be an avenue to assist in opening up the United States to be closer to business as usual.”

“The FDA’s EUA is recognition that the Qorvo Omnia platform can help address the ongoing need for rapid, accurate and clinically-reliable diagnostic testing,” added James Klein, President of Qorvo Biotechnologies. “We are honored to leverage Qorvo’s technology portfolio to help public health officials respond to this global pandemic.”

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Qorvo Biotechnologies, LLC