20/04/2026
FDA clearance #2 for Ligence! Automated LV strain now FDA-cleared. Supporting faster, more consistent echo care for patients. ❤️
By automating LV Strain, is making a "premium" clinical metric accessible to every echo lab in the US, regardless of their volume or staffing levels. It’s no longer about whether a clinician has the time; it’s about the patient getting the best diagnostic data possible.
Fantastic news! Congratulations! 👏
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Lithuania, April 14th, 2026 – Ligence announces it has received its second U.S. Food and Drug Administration (FDA) 510(k) clearance for the newest iteration of its AI-powered echocardiography software, Ligence Heart. Building on its initial clearance, the updated platform now features fully automa...