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.

NeuroMatch is a cloud-based medical software developed by LVIS Corporation to assist neurologists in reviewing and analyzing EEG recordings by automatically detecting potential seizures and epileptiform spikes. It employs advanced AI algorithms to highlight important EEG events, helping clinicians interpret brain activity more efficiently without providing a direct diagnosis.

FDA #
K241390
Product Code

The REMI-AI Rapid Detection Module (REMI-AI RDM) is an AI-based seizure detection software integrated into the REMI Remote EEG Monitoring System. It analyzes EEG data in near real-time to notify clinicians of potential electrographic seizures, aiding in patient evaluation by marking events in the EEG record. It is intended for use in non-ICU healthcare settings with adult and pediatric patients (6+ years).

FDA #
K240408
Product Code

The CEREGLIDE 42 and 57 Intermediate Catheters, together with the Cerenovus Aspiration Tubing Set, are medical devices used to remove blood clots from large intracranial vessels during acute ischemic strokes. These catheters are navigated through the brain's blood vessels under fluoroscopic imaging to restore blood flow by aspirating clots, helping patients who cannot receive or have failed drug-based clot dissolving treatments.

FDA #
K241221
Product Code

Encevis (2.1) is a software tool that assists neurologists by automatically analyzing EEG recordings to detect seizures, spikes, electrographic status epilepticus, and other brain activity patterns. It reduces artifacts in EEG data, provides quantitative measures like frequency bands and burst suppression, and displays alerts to support rapid clinical decision-making, especially in acute care settings.

FDA #
K240993
Product Code
OMB

autoSCORE is a software tool that assists neurologists by automatically analyzing EEG recordings to identify and categorize abnormal brain activity such as epileptiform and non-epileptiform abnormalities. It acts as a decision support system, marking potential abnormal areas on EEG data, thereby helping clinicians review EEGs more efficiently and accurately. The device does not provide final diagnostic conclusions but rather supports professional judgment in interpreting EEG results.

FDA #
K231068
Product Code
OMB

The REMI AI Discrete Detection Module (REMI-AI DDM) is a software tool designed to assist physicians qualified in EEG interpretation by automatically identifying and marking sections of EEG recordings that may correspond to seizure-like events. It processes previously acquired EEG data collected via the REMI Remote EEG Monitoring System, helping speed up and improve the review process for EEG data in patients aged 6 years and older. The software does not provide diagnostic conclusions but serves as an aid to clinicians in seizure detection support.

FDA #
K231779
Product Code
OMB

The Ceribell Status Epilepticus Monitor is a software medical device that analyzes EEG data captured from a headband device to automatically detect electrographic status epilepticus in patients at risk of seizures. It provides timely diagnostic support to clinicians in acute care environments, enabling faster treatment decisions for this critical neurological condition.

FDA #
K223504
Product Code
OMB

EnsoSleep is a software medical device designed to analyze previously recorded physiological signals from sleep studies to automatically score sleep stages, detect arousals, leg movements, and various types of sleep-disordered breathing events. It supports both adult and pediatric patients and can be used for in-lab or home sleep tests. EnsoSleep assists clinicians by providing automated detection and scoring of events, which are then verified and can be edited by qualified clinicians to aid in diagnosing sleep disorders.

FDA #
K210034
Product Code
OLZ

Embrace is a wearable device worn on the wrist that monitors physiological signals such as Electrodermal Activity, motion, and temperature to detect generalized tonic clonic seizures in patients with epilepsy. It helps alert caregivers by sending notifications during seizure events, assisting in timely monitoring and care for patients both at home and in healthcare facilities.

FDA #
K181861
Product Code
POS

EnsoSleep is a software tool that uses AI algorithms to analyze sleep study data, including brain waves and breathing patterns, to help physicians evaluate sleep quality and diagnose sleep-related disorders such as sleep apnea. It automates scoring of sleep stages, detection of arousals, leg movements, and breathing events, improving efficiency while requiring clinician verification.

FDA #
K162627
Product Code
OLZ
Page 1 of 110 results
1

Ready to Sharpen Your Edge?

Join hundreds of your peers who rely on RadAI Slice. Get the essential weekly briefing that empowers you to navigate the future of radiology.

We respect your privacy. Unsubscribe at any time.