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Median Technologies submits U.S. application for 510(k) clearance of eyonis® LCS

SOPHIA ANTIPOLIS, France, May 14, 2025--Regulatory News: Median Technologies (FR0011049824, ALMDT, PEA-PME scheme eligible, "Median" or the "Company"), manufacturer of eyonis®, a suite of artificial intelligence (AI) powered Software as a Medical Device (SaMD) for early cancer diagnosis, and a globally leading provider of AI-based image analyses and central imaging services for oncology drug developers, today announced it has filed an application to the U.S. Food and Drug Administration (FDA) fo

articleMedian TechnologiesMay 14, 20255/company/median-technologies/news/median-technologies-submits-us-application-for-510k-clearance-of-eyonisr-lcs-1
Median Technologies submits U.S. application for 510(k) clearance of eyonis® LCS

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lung cancer screeningcomputer aided detectionSaMDMedianlung nodulesTechnologiesU.S. Food and Drug Administrationlung cancerpivotal studiesimaging servicescancer diagnosis