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 Revolution Vibe is a computed tomography (CT) imaging system developed by GE Medical Systems. It captures detailed cross-sectional X-ray images of the body, aiding clinicians in diagnosing and monitoring various conditions with high clarity and speed.

FDA #
K250941
Product Code
JAK

Marie is a computed tomography (CT) X-Ray system designed to capture detailed cross-sectional images of the body, aiding clinicians in diagnosing and monitoring various medical conditions through advanced imaging techniques.

FDA #
K250970
Product Code
JAK

The SOMATOM go series by Siemens Medical Solutions USA, Inc., comprises advanced CT scanner systems used in radiology to produce detailed cross-sectional images of the body. These devices assist clinicians by providing high-quality computed tomography images that support diagnosis and treatment planning for various medical conditions.

FDA #
K250822
Product Code
JAK

The Philips iCT CT System is a computed tomography scanner designed for diagnostic imaging of the head, body, cardiac, and vascular regions. It produces detailed cross-sectional images by reconstructing X-ray data taken from multiple angles, aiding clinicians in diagnosing a range of conditions. The system offers updated hardware and software improvements for enhanced image quality, cybersecurity, and usability without altering its core imaging capabilities.

FDA #
K250648
Product Code
JAK

The CT Scanner TSX-501R/1 V11.1 by Canon Medical Systems Corporation is an advanced computed tomography system that uses a photon counting detector to capture high-quality cross-sectional volume images of the whole body. This system helps clinicians perform specialized studies by providing detailed imaging data to support diagnosis and treatment planning for adult patients.

FDA #
K243398
Product Code
JAK

CardIQ Suite is a non-invasive software that analyzes cardiac CT scans to visualize heart vessels, measure calcium deposits, and evaluate heart fat volume. It helps clinicians diagnose cardiovascular diseases, monitor disease progression, and plan treatment by providing detailed vessel measurements and calcium scoring from cardiac CT images.

FDA #
K243672
Product Code
JAK

SCENARIA View Phase 5.0 is a multi-slice CT system that acquires axial volumes of the whole body in various scan modes. It includes AI-based features such as AutoPose that automatically recognizes and sets scan ranges for body parts, improving workflow and scan accuracy. The system supports high-quality imaging with motion correction and provides enhanced post-processing capabilities to assist clinicians in diagnosis and interventional guidance.

FDA #
K250370
Product Code
JAK

The Spectral CT system by Philips is an advanced CT scanner that acquires dual-energy X-ray data to provide detailed cross-sectional images of the body. This technology enables the analysis of different materials' chemical composition and improves visualization of anatomical and pathological structures, aiding clinicians in diagnostic imaging and treatment planning across multiple clinical areas including radiology, cardiology, and oncology.

FDA #
K244008
Product Code
JAK

The uCT ATLAS Astound with uWS-CT-Dual Energy Analysis and uCT ATLAS with uWS-CT-Dual Energy Analysis are advanced CT imaging systems that produce cross-sectional whole-body images using X-rays. They incorporate AI-based technologies to enhance image reconstruction, reduce artifacts, and improve diagnostic quality, particularly for cardiac imaging and lung cancer screening. The systems support low dose CT for early lung nodule detection and use dual energy imaging for detailed tissue characterization.

FDA #
K243617
Product Code
JAK

The SpotLight / SpotLight Duo with Low Dose Lung Cancer Screening Option is a CT X-ray system that produces cross-sectional images of the body, particularly the cardiovascular and thoracic regions. It includes protocols for low dose CT scans aimed at lung cancer screening, ensuring minimal radiation exposure while maintaining image quality. This device assists clinicians in diagnosing lung cancer and planning related therapies, utilizing advanced image reconstruction algorithms and adaptable scan techniques for patients of various sizes.

FDA #
K250650
Product Code
JAK
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