RapidAI Extends the Reach of Deep Clinical AI with Five New FDA Clearances
SAN MATEO, Calif. — November 25, 2025 — RapidAI, the pioneer of deep clinical AI and global leader in enterprise imaging, today announced the U.S. Food and Drug Administration (FDA) clearance of five new imaging modules: Rapid DeltaFuse™, Rapid LMVO, Rapid MLS, Rapid OH, and Rapid Aortic for measurement. Together, these clearances mark a significant expansion of the Rapid Enterprise™ Platform, reinforcing RapidAI’s identity as the only platform purpose-built to bring deep clinical intelligence, seamless workflow integration, and secure IT infrastructure to hospitals worldwide.