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.

The Ahead 300 is a portable, non-invasive medical device that records and analyzes brain electrical activity to assist clinicians in evaluating patients with closed head injuries. It provides algorithm-based classifications of structural brain injury and measures brain function and cognitive performance to support diagnosis and treatment decisions, particularly to aid in deciding on the necessity of head CT scans.

FDA #
K161068
Product Code
PIW

The Triton System is a medical software application designed to assist surgical teams by estimating the amount of blood loss on used surgical sponges through image analysis. It runs on an iPad and uses validated hardware and software to calculate hemoglobin mass and blood volume, helping clinicians manage bleeding and surgical sponges more effectively during operations.

The BrainScope Ahead 200 is a portable EEG device designed to aid physicians in evaluating patients with mild traumatic brain injury by measuring and analyzing brain electrical activity. It supports clinical decision-making regarding the need for head CT scans by providing objective quantitative EEG parameters. The device is intended for use as an adjunct to standard clinical practice and includes features such as continuous impedance monitoring and cognitive assessment tools for military use. It helps clinicians by providing rapid brain activity data to support the assessment of brain injury severity without replacing imaging such as CT scans.

FDA #
K143643
Product Code
PIW

The IRIS Intelligent Retinal Imaging System is a web-based software that stores, manages, and displays retinal images and diagnostic data from computerized instruments. It allows licensed clinicians to review fundus images and visual field data to evaluate and diagnose retinal conditions such as diabetic retinopathy, glaucoma, and macular degeneration, thereby assisting in patient care and follow-up.

FDA #
K141922
Product Code
NFJ

The BrainScope Ahead 100 is a portable EEG-based device designed to assist physicians in evaluating patients with mild traumatic brain injury. It analyzes brain electrical activity to help decide if a head CT scan is needed, potentially reducing unnecessary CT scans and radiation exposure. The device processes EEG data using AI-driven algorithms to classify patients based on the likelihood of structural brain injury visible on CT.

Product Code
PIW

The BioPlex 2200 ANA Screen with Medical Decision Support Software (MDSS) is a laboratory tool that assists clinicians by analyzing patterns in antibody test results from human serum or plasma samples. Using AI principles (k-nearest neighbor algorithm), it compares patient antibody profiles against a large database to suggest associations with specific systemic autoimmune diseases such as lupus, scleroderma, Sjögren's syndrome, and polymyositis. This software helps improve diagnostic accuracy and guides additional testing decisions.

FDA #
K043341
Product Code
NVI
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