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 MIMOSA Imager is a cordless, non-contact tissue oximeter that estimates and maps oxygen saturation in superficial tissue. It captures spatially-resolved images using visible and near-infrared light and presents tissue oxygenation as a heat map on a connected Android device. This helps clinicians monitor circulatory or perfusion status in patients, especially for skeletal muscle and suspected compromised circulation.

Merge PACS is a software system that helps medical professionals view, analyze, and manage images from various medical imaging modalities such as CT, MRI, PET, ultrasound, and mammography. It supports diagnostic reading, reporting, and communication workflows, enabling clinicians to efficiently handle patient imaging studies and related data. It includes advanced image manipulation tools and workflow management features to assist radiologists and other medical staff.

FDA #
K192455
Product Code
LLZ

Syngo.Via RT Image Suite is a software tool designed to help clinicians visualize, manipulate, and contour medical images from various imaging modalities such as CT, MRI, and PET. It supports 3D and 4D image visualization and assists with the segmentation of tumors and organs-at-risk to aid in radiation therapy planning and response assessment. The software incorporates AI techniques, including deep learning-based contouring, to improve the accuracy and efficiency of treatment preparation, thereby enhancing patient care in radiation therapy.

FDA #
K192065
Product Code
MUJ

SIS Software Version 3.6.0 is an advanced medical imaging application designed to assist neurosurgeons, neurologists, and radiologists by processing MRI and CT scans to create detailed 3D models of brain structures, particularly the subthalamic nuclei. It uses machine learning to enhance images, aiding in the visualization and planning of stereotactic brain surgeries, thereby improving surgical accuracy and patient outcomes.

FDA #
K192304
Product Code
LLZ

BrainScope TBI is a portable, non-invasive device that assists clinicians in evaluating patients with mild traumatic brain injury and concussion by analyzing brain electrical activity through EEG along with cognitive tests and clinical symptoms. It helps identify the likelihood of structural brain injury and assesses brain function, supporting decisions about the need for further imaging like CT scans.

FDA #
K190815
Product Code
PIW

D2P is a software tool developed by 3D Systems that processes medical imaging data (DICOM) to create 3D segmentations and physical models. It assists clinicians in surgical planning by allowing the generation of accurate physical replicas of anatomical regions from imaging data, supporting diagnosis and treatment decisions in cardiovascular, craniofacial, gastrointestinal, genitourinary, neurological, and musculoskeletal areas.

FDA #
K183489
Product Code
LLZ

The Zio XT and Zio AT ECG Monitoring Systems by iRhythm Technologies, Inc. analyze continuous ECG data collected via wearable patches and generate detailed reports on cardiac events. These systems help clinicians diagnose heart rhythm abnormalities by providing comprehensive, beat-to-beat ECG analysis over long monitoring periods for patients with or without symptoms.

FDA #
K190593
Product Code
DQK

Biovitals Analytics Engine is a cloud-based software that analyzes continuous biometric data from sensors measuring heart rate, respiratory rate, and activity in ambulatory patients. It creates a personalized biometric signature for each patient and computes a Biovitals Index to track changes in vital signs over time, providing clinicians with additional insight for routine monitoring without replacing traditional vital sign monitoring.

FDA #
K183282
Product Code
PLB

EyeBOX is an eye-tracking device designed to help diagnose concussion by measuring and analyzing eye movements in patients within one week of a head injury. It uses near-infrared cameras to track gaze positions and an AI-driven algorithm to detect subtle changes in eye movements associated with concussion, aiding clinicians in neurological assessment.

FDA #
K191183
Product Code
QEA

KIDScore D3 is an AI-based decision support tool designed to aid embryologists in assessing the viability of embryos on Day 3 by scoring their likelihood to develop to the blastocyst stage. It integrates with the EmbryoScope timelapse incubator systems and helps clinicians select embryos for transfer, freezing, or continued development, enhancing decision-making in assisted reproduction procedures.

FDA #
K182798
Product Code
PBH
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