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 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

RadUnity (Version 1.0.0) is a software device designed to centralize, manage, standardize, and network CT images using the DICOM protocol. It reformats CT medical images according to user-defined preferences to ensure consistent image formatting, thus supporting qualified radiology professionals in preparing images for interpretation. It is not intended for primary diagnostic review nor for mammographic image interpretation.

FDA #
K242810
Product Code

BriefCase-Quantification is an AI-based software that analyzes contrast-enhanced CT scans to measure aortic diameters at key anatomical landmarks, helping clinicians assess normal and aneurysmal aortas. It processes CT images in a cloud environment, produces measurement results for review, and is intended to assist but not replace radiologist evaluations.

FDA #
K242203
Product Code

CT Collaboration Live is a software application integrated into Philips CT systems that enables real-time remote communication for consultation, training, and support via chat, audio/video calls, screen sharing, and remote control. It facilitates collaboration between CT system operators and remote clinical users but is not intended for remote diagnostic image review.

FDA #
K242329
Product Code

CORIOGRAPH Pre-Op Planning and Modeling Services is a software tool used for preoperative planning of orthopedic surgeries such as unicondylar knee replacement, total knee arthroplasty, and primary total hip arthroplasty. It generates patient-specific bone models and surgical plans based on medical imaging scans, helping surgeons plan and optimize implant placement before surgery.

FDA #
K242272
Product Code

The Mako Shoulder Application (1.0) is part of the Mako System designed to assist surgeons in reverse shoulder arthroplasty procedures by providing AI-driven, software-defined spatial boundaries using patient CT imaging. It aids in pre-surgical planning, implant placement, and intraoperative navigation, improving surgical accuracy and outcomes.

FDA #
K242373
Product Code

NeuroICH is a software tool designed to analyze non-contrast CT scans of the head using artificial intelligence to detect signs of intracranial hemorrhage. It provides notifications to specialist clinicians via a mobile app, helping to prioritize patient care without replacing standard diagnostic procedures.

FDA #
K241719
Product Code

The MEDRAD Centargo CT Injection System is an automated device used to inject contrast media and saline into patients during CT scans. It helps radiology professionals by providing controlled, precise, and programmable delivery of contrast agents, improving diagnostic imaging quality while ensuring patient safety through features like air detection and occlusion monitoring.

FDA #
K241849
Product Code

The Prophecy Surgical Planning System is a patient-specific surgical planning tool designed to aid orthopedic surgeons in total ankle replacement surgeries. It leverages medical imaging data from CT scans and X-rays to create customized 3D planning reports and guides that assist in the precise positioning and alignment of ankle implant components during surgery, improving surgical accuracy and patient outcomes.

FDA #
K241999
Product Code

The Caduceus S is an augmented reality-based navigation system designed to assist surgeons in accurately placing pedicle screws during percutaneous spine surgery. It leverages intraoperative CT or 2D/3D C-arm imaging and optical tracking, projecting navigation data directly into a headset worn by the surgeon to improve precision and visualization during procedures involving the thoracic and lumbosacral spine.

FDA #
K242271
Product Code
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