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 people actually have lung cancer, the device will correctly identify about 93 of them. In other words, the device reliably detects cancer when it is present. 
  • 92.4% specificity, which means that if 100 people don’t have lung cancer, the device will correctly identify about 92 of them as cancer-free. In other words, the device largely avoids false alarms. 
  • 99.9% negative predictive value, which means that if the device says you don’t have cancer, there’s a 99.9% chance you truly don’t have it. In other words, a negative result is highly reliable. 

These outcomes demonstrate the powerful potential for eyonis LCS to be used as a tool to enhance lung screening programs by improving screening accuracy, while reducing unnecessary follow-up procedures. The ability to detect suspicious pulmonary nodules earlier may also help clinicians diagnose lung cancer at earlier stages more frequently, where patient outcomes can be significantly improved. 

If you or a loved one is eligible for lung cancer screening, ask your healthcare team about eyonis LCS. For questions about lung cancer treatments, trials, or biomarker testing, contact our LungMATCH team at support@go2.org or 1-800-298-2436.   

Read the FDA approval.