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 software that helps hospitals quickly identify and prioritize urgent head CT angiography scans with possible M1 Large Vessel Occlusion. It analyzes images and sends notifications with preview images to clinicians, enabling faster triage without replacing standard image interpretation.

FDA #
K221314
Product Code
QAS

Rapid LVO is a software device designed to analyze CT angiography images of the head to help healthcare providers identify suspected large vessel occlusions quickly. By flagging possible cases of ICA or MCA-M1 occlusion and providing notifications with preview images, it supports faster triage and prioritization of medical images, aiding timely clinical decision-making in stroke care.

FDA #
K221248
Product Code
QAS

BriefCase by Aidoc Medical is an AI-powered software that analyzes non-enhanced head CT images to identify potential intracranial hemorrhage. It assists clinicians by flagging suspect cases and sending notifications with preview images to help prioritize patient care workflow. It operates alongside standard imaging interpretation without altering original medical images.

FDA #
K221240
Product Code
QAS

The EFAI RTSuite CT HN-Segmentation System is AI-powered software designed to assist radiation oncology professionals by automatically contouring organs at risk in head and neck CT images. It helps streamline radiation therapy treatment planning by providing initial segmentations that clinicians review and edit, improving workflow efficiency and accuracy.

FDA #
K220264
Product Code
QKB

AI-Rad Companion Brain MR is software that assists clinicians by automatically analyzing brain MRI scans. It segments various brain structures, quantifies their volumes, and highlights white matter hyperintensities, comparing results to normal data. This helps radiologists make more accurate and efficient evaluations of brain health.

FDA #
K213706
Product Code
QIH

MRCAT Head & Neck is a software tool integrated into Philips MR systems that automatically processes MRI data to create synthetic CT-like images for radiation therapy treatment planning in patients with soft tissue tumors in the head and neck region. It helps clinicians accurately estimate radiation dose distributions without needing a separate CT scan, improving planning precision and patient care.

FDA #
K214081
Product Code
MUJ

BriefCase is an AI-powered software that analyzes head CT Angio (CTA) images to assist clinicians by flagging suspected Brain Aneurysm cases above 5 mm, helping prioritize urgent cases and improving workflow efficiency. It provides notifications and preview images but is not intended for primary diagnosis, supporting clinicians to review images faster and potentially reduce time to treatment.

FDA #
K213721
Product Code
QAS

Viz ANEURYSM is an AI-powered software that analyzes CT angiogram images of the head to detect suspected aneurysms of at least 4mm. It helps radiologists prioritize patient studies by flagging and highlighting cases with suspected aneurysms in a standalone application. This assists in faster triage and review, improving workflow efficiency while ensuring diagnostic decisions remain with the radiologist.

FDA #
K213319
Product Code
QFM

Rapid is a medical image processing software that helps clinicians visualize and analyze tissue changes in CT and MRI images, particularly aiding in the selection of acute stroke patients for treatment. It uses AI/ML components to detect image artifacts and supports advanced imaging features such as perfusion, diffusion and dynamic contrast analysis.

FDA #
K213165
Product Code
LLZ

syngo.CT Brain Hemorrhage is an AI-driven software that assists radiologists by analyzing non-contrast head CT scans to prioritize cases suspicious for acute intracranial hemorrhage. It flags findings to improve workflow efficiency by enabling faster review of urgent cases but is not intended for standalone diagnosis.

FDA #
K203260
Product Code
QAS
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