FDA Clears eyonis LCS for Use in Lung Cancer Screening

2026-02-18T07:14:14-06:00February 18th, 2026|Hot Topics, News, Science and Research|

On February 6th, 2026, the U.S. Food and Drug Administration (FDA) approved Median Technologies’ eyonis Lung Cancer Screening (LCS), a medical device used for the combined detection and diagnosis of lung cancer. eyonis LCS is an AI-based technology designed to support the earlier detection of lung cancer by helping clinicians identify and characterize pulmonary (lung) nodules on low-dose CT (LDCT) scans.   In performance testing, eyonis LCS demonstrated a:   93.3% sensitivity, which means that if 100 [...]

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