Established market leader in stroke AI imaging receives its first FDA clearance in the lung imaging space. With this expanded foundation of AI-driven healthcare solutions, the Oxford-based company remains committed to driving innovation and delivering impactful advancements in imaging biomarkers.
Brainomix announced FDA 510(k) clearance for its e-Lung AI software, a breakthrough that marks its first FDA clearance in lung imaging and extends the company's AI imaging portfolio beyond stroke. e-Lung is powered by Brainomix's proprietary weighted reticulovascular score (WRVS) imaging biomarker, designed to support earlier diagnosis and clinical assessment in interstitial lung disease (ILD), including idiopathic pulmonary fibrosis (IPF).