FDA Clears eyonis LCS for Use in Lung Cancer Screening
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 [...]