eyonis Inc., a Median Technologies Company, to Present Study Results Supporting eyonis® LCS Performance Claims at CHEST 2026

S. subsidiary, will participate in the CHEST 2026 Annual Meeting, the annual scientific meeting of the American College of Chest Physicians, taking place October 18-21, 2026, in Phoenix, Arizona. A key highlight of the conference will be the presentation of results from the study used to establish the performance claims of eyonis® LCS, Median Technologies' flagship Software as a Medical Device (SaMD) for lung cancer screening. The presentation will provide the CHEST medical community with detailed insights into the clinical performance of the device, which received FDA 510(k) clearance in February 2026 and is commercially available in the United States.

CHEST offers an important forum to engage with pulmonologists, who play a key role in lung cancer screening programs and represent an important stakeholder group for the adoption of AI-enabled support solutions in clinical practice. “CHEST is one of the leading scientific meetings for the pulmonology community and an important venue to present the existing clinical evidence supporting eyonis® LCS,” said Oran Muduroglu, President of eyonis Inc.

” Scientific Presentation at CHEST 2026 The abstract, “Artificial Intelligence for Lung Cancer Screening: Patient-Level Performance of a Computer-Aided Detection/Diagnosis Software as a Medical Device,” will be presented by Benoit Huet, PhD, Senior Vice President, AI Engineering and Research at Median Technologies. The research includes co-authors from Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France, and Brigham and Women's Hospital, Boston, Massachusetts. m. m.

9% negative predictive value. The findings suggest that eyonis® LCS helps reduce both false positives and false negatives (missed cancers) while supporting more consistent clinical decision-making in lung cancer screening programs through the combination of computer-aided detection and nodule-specific malignancy assessment. Demonstrating eyonis® LCS at Booth #1221 Throughout the conference, the eyonis® team will be available at Booth #1221 to demonstrate eyonis® LCS and discuss its role in supporting lung cancer screening programs.

eyonis® LCS is the first and only FDA-cleared AI/ML-based Software as a Medical Device that combines computer-aided detection and computer-aided diagnosis within the lung cancer screening workflow. The software provides healthcare professionals with both nodule detection capabilities and a nodule-specific malignancy score, supporting clinical decision-making from nodule identification through patient management. Supporting the Commercial Deployment of eyonis® LCS in the United States Participation in CHEST 2026 is part of the Company’s strategy to support the commercial deployment of eyonis® LCS in the United States.

Following FDA 510(k) clearance obtained in February 2026, the Company continues to engage with key stakeholders across the lung cancer screening ecosystem, including pulmonologists, radiologists, screening centers and healthcare systems. About Median Technologies: Pioneering innovative software as a medical device and imaging services, Median Technologies harnesses cutting-edge AI to enhance the accuracy of early cancer diagnoses and treatments. Median's offerings include iCRO, which provides medical image analysis and management in oncology trials, and eyonis®, an AI/ML tech-based suite of software as a medical device (SaMD).

Median empowers biopharmaceutical entities and clinicians to advance patient care and expedite the development of novel therapies. S. and China, trades on the Euronext Growth market (ISIN: FR0011049824, ticker: ALMDT). For more information, visit Forward-Looking Statements This press release contains forward-looking statements.

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