Tempus Partners with Median Technologies to Integrate FDA-Cleared AI Lung Cancer Screening Tool
核心洞察
Tempus AI has announced a collaboration with Median Technologies (搜索) to integrate the FDA-cleared eyonis® LCS (搜索) AI-powered lung cancer screening device into its Tempus Pixel (搜索) platform.
The eyonis® LCS (搜索) system demonstrates 93.3% sensitivity, 92.4% specificity, and 99.9% negative predictive value for detecting and characterizing lung cancer in low-dose CT scans.
Only 20% of eligible Americans were screened for lung cancer in 2024, and achieving full participation could prevent an estimated 62,110 lung cancer deaths over five years.
Tempus AI has announced a strategic collaboration with Median Technologies (搜索) to integrate the recently FDA-cleared eyonis® LCS (搜索) artificial intelligence-powered lung cancer screening device into its Tempus Pixel (搜索) platform. The partnership aims to address the significant gap in lung cancer screening participation and improve early detection capabilities across the United States.
AI-Powered Screening Technology
eyonis® LCS (搜索) is an AI-based Computer-Aided Detection and Diagnosis (CADe/CADx) Software as a Medical Device (SaMD) that received FDA 510(k) clearance on February 9, 2026. The system is uniquely capable of both detecting and characterizing lung cancer in low-dose CT scans (LDCT) with impressive performance metrics: 93.3% sensitivity, 92.4% specificity, and 99.9% Negative Predictive Value (NPV), based on manufacturer values calculated on a lung cancer screening reference population.
The technology enables clinicians to not only detect lung nodules but also characterize and risk stratify them from the same CT image without additional workflow steps. This integration provides a proprietary nodule malignancy score that allows clinical teams to stratify and prioritize patients in lung cancer screening programs.
Addressing Critical Screening Gaps
According to a study by the American Cancer Society cited in the announcement, only about 20% of eligible individuals in the U.S. were screened for lung cancer in 2024. The collaboration aims to close this significant gap, with full participation among eligible individuals potentially preventing an estimated 62,110 lung cancer deaths over five years.
The partnership targets the 14.5 million Americans eligible for lung cancer screening and builds on the existing NT-APC 1508 reimbursement pathway, which provides coverage of $601-$700 for screening procedures.
Platform Integration and Market Access
Through this non-exclusive distribution agreement, Tempus AI will distribute eyonis® LCS (搜索) to U.S. imaging providers through the Tempus Pixel (搜索) platform and support implementation, customer onboarding, and workflow integration. Tempus Pixel is an FDA-cleared, CE-marked AI-enabled solution that offers advanced analysis, tools, and automated reporting from radiology images to help providers accurately track and quantify lesions.
"Activating our distribution collaboration with Tempus AI is a decisive step in bringing eyonis® LCS (搜索) to patients at national scale," stated Fredrik Brag, CEO and Founder of Median Technologies (搜索). "Tempus AI's strong leadership in AI-enabled precision medicine, deeply integrated data-technology ecosystem, and strong market presence make them an exceptional partner to drive rapid and high-impact adoption of eyonis® LCS across the United States."
Strategic Vision and Future Expansion
Razik Yousfi, Tempus SVP & GM, AI Products, emphasized the clinical impact of the collaboration: "We believe AI reaches its full potential when it helps clinicians identify disease earlier and more accurately. By expanding our Pixel platform with sophisticated lung cancer screening AI tools, we are enabling radiologists to manage complex caseloads while prioritizing early-stage detection. Our collaboration with Median Technologies (搜索) is about more than technology; it's about improving the standard of care and preventing avoidable deaths through better screening access."
Revenues generated from the use of eyonis® LCS (搜索) will be shared between the parties according to the commercial terms of the partnership. Median Technologies (搜索) continues to progress along the European regulatory pathway for eyonis® LCS and anticipates obtaining CE marking in Q2 2026, with Tempus AI supporting the commercial rollout across Europe under the executed distribution agreement.
Company Background and Capabilities
Tempus has significantly expanded its diagnostic capabilities through strategic acquisitions, including Arterys in 2022, which incorporated AI-driven imaging tools ranging from lung CTs and chest X-rays to cardiac MRIs. This was followed by the acquisition of Paige, which contributed a proprietary dataset of almost 7 million clinically annotated, de-identified pathology slides to accelerate Tempus' AI development efforts.
Median Technologies (搜索), based in France with presence in the U.S. and China, specializes in innovative software as medical devices and imaging services, harnessing AI to enhance the accuracy of early cancer diagnoses and treatments. The company trades on the Euronext Growth market under the ticker ALMDT.