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.

BriefCase by Aidoc Medical, Ltd. is an AI-based radiology triage and notification software designed to assist radiologists by automatically analyzing head CT and chest CT pulmonary angiogram (CTPA) images. It detects suspected cases of Intracranial Hemorrhage and Pulmonary Embolism, providing timely notifications and compressed preview images to prioritize urgent cases. This facilitates faster review and potentially improves patient outcomes by allowing earlier intervention, while not replacing standard diagnostic processes.

FDA #
K190072
Product Code
QAS

cmTriage is a software tool that uses artificial intelligence to analyze 2D digital mammograms and flags suspicious cases to help radiologists prioritize which exams to review first. It integrates with the Picture Archiving and Communication System (PACS) worklist but does not alter images or provide diagnostic results. cmTriage aims to improve the efficiency of breast cancer screening workflows by identifying potentially abnormal cases for quicker attention.

FDA #
K183285
Product Code
QFM

Accipiolx is an artificial intelligence software tool designed to automatically analyze non-contrast head CT scans to detect signs of acute intracranial hemorrhage. It integrates into hospital radiology networks to prioritize cases suggesting hemorrhage, enabling quicker review by clinicians and faster treatment decisions in acute care settings.

FDA #
K182177
Product Code
QAS

BriefCase is an AI-powered software that assists radiologists by analyzing non-enhanced head CT images to detect suspected intracranial hemorrhages. It provides timely notifications with preview images to prioritize cases for faster review, helping clinicians improve workflow efficiency and patient care without altering original images or making diagnoses.

FDA #
K180647
Product Code
QAS

The NuVasive Pulse System is an advanced surgical device designed to assist surgeons during spinal procedures by monitoring neurophysiologic activity and providing enhanced fluoroscopic imaging and navigation. It combines neurophysiologic monitoring to assess nerve function and safety, image enhancement to improve the quality of fluoroscopic images at low doses, and computer-assisted navigation to guide precise placement of spinal implants, helping to improve surgical accuracy and patient outcomes.

FDA #
K180038
Product Code
OLO
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