FDA Radiology AI Devices

Discover FDA-cleared medical imaging AI devices with clean summaries, company insights, and linked references. We help you quickly understand what's approved, who built it, and how it fits into the evolving landscape of radiology AI.

Showing 1617 FDA devices.

Op.n Navigation by Ecential Robotics is a surgical navigation system designed to assist surgeons during spinal surgery. It uses intra-operative 3D imaging to help accurately position surgical instruments and implants like pedicle screws in the thoracolumbar spine. This technology improves surgical precision and patient outcomes by providing real-time navigation based on detailed imaging.

FDA #
K242914
Product Code
OLO

The SPINEART Navigation Instrument System is a surgical tool used in thoracolumbar spinal surgery to help surgeons accurately locate anatomical structures for the placement of spinal screws. It integrates with the eCential Op.n PERLA® TL Navigation System, which uses intraoperative 3D imaging, to improve surgical precision in both open and minimally invasive procedures.

FDA #
K242890
Product Code
OLO

The Intra-Operative Positioning System (IOPS®) is a surgical navigation tool that helps clinicians navigate catheters and guidewires during endovascular procedures. It uses pre-acquired 3D vascular imaging data combined with real-time electromagnetic tracking to display precise tip positioning, serving as an adjunct to fluoroscopy. This technology enhances procedural accuracy without making direct diagnoses.

FDA #
K243842
Product Code
DQK

LVivo Seamless is a software platform designed to automatically process echocardiogram ultrasound images to detect, measure, and calculate important cardiac medical parameters. It helps clinicians by selecting the appropriate image clips and activating AI modules to evaluate ejection fraction (EF) and global longitudinal strain (GLS), improving workflow and providing quantitative cardiac function data for better diagnosis and monitoring.

FDA #
K243331
Product Code
QIH

The Philips IntelliSite Pathology Solution 5.1 is an automated system that creates, views, and manages digital images of pathology slides prepared from tissue samples. It aids pathologists by providing digital visualization of glass slides, facilitating the review and interpretation of surgical pathology in a digital format, thus modernizing and streamlining pathology workflows.

FDA #
K243871
Product Code
PSY

The Mako Total Hip Application 5.0 is a surgical assistive system that uses CT image data to create a 3D model of a patient's hip anatomy, helping surgeons plan and perform total hip replacement surgeries with high precision. It incorporates a robotic arm and software to guide implant placement within software-defined boundaries, improving surgical accuracy and patient outcomes.

FDA #
K243751
Product Code
OLO

Prostate MR AI (VA10A) is a plug-in AI software device designed to assist radiologists in interpreting prostate MRI scans. It automatically segments the prostate gland, detects suspicious lesions, and assigns scores to help radiologists identify and classify potential prostate cancer. This tool supports clinicians by augmenting their workflow and improving diagnostic accuracy.

FDA #
K241770
Product Code
QDQ

Ceevra Reveal 3+ is a software medical device that processes 3D images from CT and MR scans, employing machine learning to generate segmentations of normal anatomy. It helps healthcare professionals in preoperative surgical planning and intraoperative visualization to improve patient management. The software runs on computers and mobile devices and provides interactive tools for clinicians to examine anatomical structures in detail.

FDA #
K243933
Product Code
QIH

HeartSee Cardiac P.E.T. Processing Software is a tool that helps trained clinicians analyze heart PET images to quantify blood flow and heart function. It provides detailed maps and measurements that assist in diagnosing coronary artery disease by measuring myocardial perfusion and coronary flow reserve. This enables better clinical interpretation and patient management based on quantitative PET imaging data.

FDA #
K243881
Product Code
KPS

JLK-SDH is an AI-powered software that analyzes non-contrast CT head images to detect suspected subdural hemorrhage (SDH). It assists radiologists by notifying them of potential cases in a parallel workflow to standard care, enabling quicker communication and prioritization for specialist review. This helps clinicians promptly identify and manage patients with SDH, improving workflow efficiency and potentially patient outcomes. The device is intended for notification purposes only and does not replace diagnostic evaluation.

FDA #
K243611
Product Code
QAS
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