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Sekisui and Aptitude Partner on POC, At-Home COVID Tests

Sekisui formalized an exclusive distribution agreement with Aptitude Medical Systems to sell the Aptitude Metrix COVID Test in the U.S.

Daxor submitted its next-generation blood volume analyzer—Daxor BVA—to the U.S. FDA via the 510(k)/CLIA-waiver dual submission pathway.

Posted by Andy Lundin | Dec 27, 2023 | Covid 19 |

Co-Diagnostics submitted its Co-Dx PCR COVID-19 test for review by the U.S. FDA for Emergency Use Authorization (EUA).

The company began commercial shipments as part of the initial purchase order for 2.5 million tests, with further shipments scheduled.

QuidelOrtho received 510(K) clearance from the FDA for its innovative Savanna PCR platform and Savanna HSV 1+2/VZV in vitro diagnostic test