Computer-aided detection (CAD) developer iCAD said its PowerLook Tomo Detection software has received premarket approval (PMA) from the U.S. Food and Drug Administration (FDA).
PowerLook Tomo Detection is concurrent-read CAD software for digital breast tomosynthesis (DBT). It automatically analyzes each tomosynthesis plane and identifies suspicious areas, which are blended onto a 2D synthetic image to provide radiologists with a single enhanced image, the firm said.
PowerLook Tomo Detection is currently available on GE Healthcare DBT systems. It received the CE Mark and Health Canada approval in 2016 and is currently being used by multiple breast imaging centers in Europe, according to iCAD.













![A normal mammogram confirmed by three-year radiologic follow-up illustrates reader-marked regions of interest (ROIs) during (A) unaided (round 1) and (B) artificial intelligence (AI)–assisted (round 2) reading. Each colored dot represents an ROI for recall by a human reader. Readers could mark more than one ROI per case, represented by multiple dots of the same color. During AI-assisted reading, the AI system displayed three visible prompts: two with suspicion of malignancy scores of 35% (left mediolateral oblique [L MLO] and craniocaudal [L CC]) and one with a suspicion of malignancy score of 10% (right craniocaudal [R CC]), shown as polygonal overlays. Without AI, six of 10 readers (60%) marked a false-positive ROI. With AI assistance, this fell to two of 10 (20%). R MLO = right mediolateral oblique.](https://img.auntminnie.com/mindful/smg/workspaces/default/uploads/2026/07/2026-07-14-radiology-mammogram-ai-auto-bias.H0bYO8QlWs.jpg?auto=format%2Ccompress&fit=crop&h=112&q=70&w=112)





