April 20, 2026- QuidelOrtho Corporation announced it has completed the acquisition of LEX Diagnostics (“LEX”) for cash consideration of approximately $100 million. The LEX VELO System received U.S. Food and Drug Administration (“FDA”) 510(k) clearance and CLIA waiver in February 2026.
The LEX VELO System is a breakthrough molecular diagnostics platform that is designed to deliver highly sensitive, multiplex RT-PCR testing for Influenza A, Influenza B and COVID-19 directly from a swab sample in approximately six to ten minutes. Its proprietary cartridge-based design supports rapid clinical decision-making in decentralized care environments by eliminating the need for external liquid handling; delivering speed, reliability and ease of use. The acquisition of LEX marks a critical milestone in QuidelOrtho’s molecular diagnostics strategy to accelerate its growth in point-of-care molecular diagnostics by acquiring innovative technology within one of the fastest-growing segments of the diagnostics market.
Completing the acquisition of LEX expands QuidelOrtho’s molecular diagnostics portfolio while complementing the Company’s leadership positions in immunoassay, clinical chemistry and transfusion medicine. It reinforces QuidelOrtho’s ability to deliver integrated diagnostic solutions across the continuum of care, from point of care to hospital, lab to clinic.
QuidelOrtho expects to initiate the U.S. commercial launch of the LEX VELO System later this year. Global expansion is expected to follow, subject to local regulatory approvals.
QuidelOrtho is dedicated to advancing diagnostics to power a healthier future. For more information, visit quidelortho.com.
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