The new director at the FDA overseeing medical devices will confront criticisms about hasty approvals as she ushers in ...

Cad (Nasdaq:ICAD) announced today that the FDA cleared its ProFound Detection version 4.0 for digital breast tomosynthesis ...

Dr. Michelle Tarver, a veteran of the Food and Drug Administration (FDA), has taken charge of the FDA’s device division at a ...

As of August 2024, the FDA has greenlit a staggering 950 AI– and ML-enabled medical devices. With the surge of connected ...

Discover how Remedy Logic's FDA-cleared RAI program, powered by AI, is revolutionizing spine MRI interpretation for radiologists and patients.

FDA and the Department of Veterans Affairs (VA) announced last week that they plan to develop the first intergovernmental health ...

FDA Commissioner Robert Califf calls it the “first intergovernmental health AI laboratory” that will test AI. The FDA ...

NASHUA, N.H., Nov. 12, 2024 (GLOBE NEWSWIRE) -- iCAD, Inc. (NASDAQ: ICAD) (“iCAD” or the “Company”) a global leader in clinically proven ...

Know more about the VA and FDA's initiative to provide a safe and secure laboratory for evaluating AI technologies designed ...

Over the past decade, FDA approvals of artificial intelligence and machine learning (AI/ML)–enabled medical devices have surged. They reached a ...

Zeta Surgical announced that the FDA granted 510(k) clearance for its Zeta Navigation System for expanded capabilities.

FDA clearance of HG202 marks a significant milestone for CRISPR/Cas13 RNA-editing in clinical applications for nAMD. The ...