Continuing its momentum in AI-powered MR, Philips has received FDA 510(k) clearance for SmartSpeed Precise [1] MR’s latest deep learning reconstruction software, marking a major milestone in the journey toward autonomous, personalized MRI. SmartSpeed Precise is the industry's first integrated dual AI solution, delivering up to 3x faster scanning [2] and up to 80% sharper images [3]—all in just one click.

 Unveiled at ECR 2025, SmartSpeed Precise is now cleared for clinical use across Philips’ entire portfolio of 1.5T and 3.0T MRI systems [4], including its extensive installed base. This makes it one of the most scalable and impactful innovations in the MRI market today.

“This FDA clearance is a powerful validation of Philips’ leadership in AI-powered MRI innovation,” said Ioannis Panagiotelis, PhD, Business Leader MR at Philips. “SmartSpeed Precise reflects our commitment to continuous innovation that addresses clinicians' real-world pressures. By integrating dual AI with our proven Compressed SENSE engine, we are enabling faster, sharper, and smarter MR scans—making high-quality imaging more accessible and efficient than ever before.”

 

Source: philips.com

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