ECHELON Synergy MRI System

by FUJIFILM Healthcare Corporation  · Based in United States → — Redefining Speed and Efficiency in MRI with AI-Powered Innovation
Radiology

Not publicly available
Regulatory Status Disclosed

Overview

The ECHELON Synergy MRI System by FUJIFILM Healthcare Corporation is a state-of-the-art 1.5 Tesla (T) magnetic resonance imaging system designed to enhance diagnostic capabilities, improve workflow efficiency, and maximize patient comfort. It features a 1.5T superconducting magnet within a wide 70cm bore and a 62cm wide table, accommodating patients up to 550 lbs. The system incorporates Fujifilm’s proprietary Deep Learning Reconstruction (DLR) technology, Synergy DLR, which is powered by artificial intelligence (AI) to deliver sharper images and significantly reduce scan times, by up to 50% compared to previous generations.

Key innovations include Synergy Vision with StillShot AI for real-time motion correction, mitigating artifacts without requiring rescans, and Synergy DLR Clear to address truncation artifacts. Patient experience is further improved with SoftSound™ gradient technology, which reduces acoustic noise by up to 96%, and an anti-bacterial Hydro AG coating on high-contact surfaces to minimize healthcare-associated infections (HAIs). The system also offers automated workflow features like AutoExam One Touch for brain and knee exams, AutoPose, and AutoSet, streamlining operations and increasing throughput. Designed for flexible siting and low power consumption, ECHELON Synergy aims for an affordable total cost of ownership.

Reviewed by Pouyan Golshani, MD — Interventional Radiologist

Key Features

  • 1.5T Superconducting Magnet with 70cm Wide Bore
  • AI-powered Synergy DLR (Deep Learning Reconstruction) for enhanced image quality and speed
  • Synergy Vision with StillShot AI for real-time motion correction
  • SoftSoundu2122 Gradient Technology for up to 96% acoustic noise reduction
  • AutoExam One Touch operation for automated brain and knee exams
  • Hydro AG antibacterial coating on high-contact surfaces
  • IP-RAPID (IterativeRAPID) for accelerated imaging with noise reduction
  • SmartECO for minimized power consumption and operating costs
  • SmartSPACE for flexible and compact installation layout
  • Dual Touch Panels for operator convenience

Use Cases

  • Diagnostic imaging of the head, body, and extremities
  • Neuro imaging (e.g., 5-minute brain exams)
  • Orthopedic imaging
  • Body imaging
  • Breast and prostate imaging
  • Vascular and cardiac imaging

What Physicians Need to Know

DICOM Support & Standards
As a modern MRI system, the ECHELON Synergy is designed to be fully DICOM compliant for seamless image transfer and interoperability with other medical imaging systems.
PACS Integration Method
The system is expected to integrate with Picture Archiving and Communication Systems (PACS) through standard DICOM protocols, allowing for efficient storage, retrieval, and viewing of images within a healthcare enterprise.
Reading Room Workflow Impact
The ECHELON Synergy significantly streamlines workflow with automated features like AutoPose (for breast, hip, spine, brain, and knee exams) and AutoExam One-Touch assessments, reducing manual steps and overall examination times. Its Synergy Vision with StillShot AI corrects motion-affected raw data in real-time, eliminating the need for repeat sequences and improving image diagnostic quality. DLR Clear, an AI-based algorithm, reduces truncation artifacts without extending scan time. Dual gantry-mounted monitors further accelerate patient preparation.
AI Model Architecture (deep learning approach)
The system incorporates Fujifilm's proprietary Synergy DLR (Deep Learning Reconstruction) technology, which utilizes AI through deep learning to enhance image clarity and expedite scanning. It also features StillShot AI for real-time motion correction and DLR Clear, a new AI-based algorithm for truncation artifact reduction. Deep Learning enhanced AutoPose is used for automated slice selection in breast, hip, and spine imaging.
Processing Speed (per study)
Synergy DLR technology reduces scan time by up to 50% compared to previous generations, with brain exams taking as little as five minutes. AI-powered reconstruction can deliver scans up to four times faster than standard scans, contributing to higher throughput.
FDA Clearance Pathway (510k/De Novo)
The ECHELON Synergy MRI System received 510(k) clearance from the US Food and Drug Administration (FDA) in August 2023.
Supported Modalities
The ECHELON Synergy is a 1.5 Tesla (1.5T) Magnetic Resonance Imaging (MRI) system, designed for imaging the head, body, spine, and extremities.
Sensitivity & Specificity Data
Specific sensitivity and specificity data for the AI algorithms or diagnostic capabilities of the ECHELON Synergy MRI System were not explicitly detailed in the provided information.
Physician Tip

For radiologists, the ECHELON Synergy's AI-powered Deep Learning Reconstruction (DLR) and artifact reduction tools like DLR Clear and StillShot can significantly enhance image quality, allowing for more confident diagnoses even in challenging cases involving patient motion or truncation artifacts. The accelerated scan times, particularly for brain exams, can improve patient throughput and reduce wait times, positively impacting patient experience and departmental efficiency. Technologists will benefit from automated workflows (AutoExam One-Touch, AutoPose) that reduce manual steps, allowing more focus on patient comfort and care.

The ECHELON Synergy MRI System is built for seamless integration into existing radiology ecosystems through its DICOM compliance. This ensures that images and patient data can be efficiently transferred to and from PACS, RIS (Radiology Information Systems), and other hospital information systems. Its open architecture design further supports potential future integrations and upgrades, ensuring long-term compatibility and adaptability within a dynamic healthcare IT environment.

Details

Category Radiology & Imaging AI
Pricing Not publicly available — N/A
DeploymentOn-premise (physical medical equipment)
Compliance
BAA AvailableUnknown AI-estimated
HIPAA CompliantUnknown AI-estimated
FDA Status 1 AI-estimated

The ECHELON Synergy MRI System received FDA 510(k) clearance (K241429) on August 13, 2024. It is intended to provide physiological and clinical information non-invasively for diagnosis by trained physicians.

Integrations
EHR Not specified
Specialties Radiology

What the Web Says

The FUJIFILM ECHELON Synergy MRI System is a 1.5T superconducting MRI system that has received FDA clearance. It is designed to provide physicians with physiological and clinical information non-invasively and without ionizing radiation. The system incorporates AI-powered algorithms and advanced technologies focused on artifact reduction and improved image quality, particularly with its latest version, v10.0.

Overall: Positive

Strengths

  • Utilizes AI-powered algorithms for faster scans and improved image resolution, especially in neurology and oncology diagnostics.
  • Features like Synergy DLR Clear and Synergy Vision are geared towards mitigating common challenges with artifacts, including truncation and motion artifacts.
  • Includes StillShot artificial intelligence (AI) for mitigating motion artifacts through real-time tracking and correction of motion-compromised raw data.
  • Offers automated slice positioning with AutoPose for Spine, Breast, and HipJoint.
  • Provides clear, high-quality images with reduced motion artifact through the application of RADAR radial sequence with iterative iRCM IP-Recon processing.
  • Upgraded standard software features with version 10 are provided to current customers free of charge.

Limitations

  • Limited publicly available reviews and opinions from physicians, healthcare IT, tech reviewers, Reddit, G2, and Capterra.
  • No reviews yet on some community rating platforms.

Based on reviews from: FUJIFILM Healthcare - Physician Ai Tools, ECHELON Synergy - Physician Ai Tools, ECHELON Synergy MRI system | FUJIFILM Healthcare Corporation, Artifact Reduction Drives Technology Advances with Updated Version of Echelon Synergy MRI System | Diagnostic Imaging, ECHELON Synergy V10.0 (K233687) u2014 FDA 510(k) | Innolitics, ECHELON Synergy (K251386) u2014 FDA 510(k) | Innolitics, September 17, 2025 Fujifilm Corporation Chaitrali Kulkarni Sr. Regulatory Affairs Specialist Fujifilm Healthcare Americas Co - accessdata.fda.gov, Magnetic Resonance Imaging Coils Market : Global Industry Analysis and Opportunity Assessment, 2036, August 13, 2024 FUJIFILM Healthcare Corporation Chaitrali Kulkarni Sr. Regulatory Affairs Specialist FUJIFILM Healthcare America, Fujifilm - Grokipedia, Search FDA-cleared listings - Radiology AI Tools Directory, Sheet1, Petition to Classify MRI Projectiles as Malfunctions | PDF | Magnetic ...

Last updated: 2026-07-18

Ratings & Reviews

No reviews yet. Be the first to review this tool!

Rate ECHELON Synergy MRI System

Clinical Value
Ease of Use
Integration
Support & Docs
Value for Money

Press & Coverage

FUJIFILM Healthcare Americas Corporation
Fujifilm Launches New ECHELON Synergy 1.5T MRI System Software with AI Powered Workflow Enhancements
FUJIFILM Healthcare Americas Corporation launched Version 10 (v10) software for its ECHELON Synergy 1.5T MRI system, featuring AI-powered enhancements like Synergy DLR Clear and Synergy Vision with StillShot to address motion artifacts and improve image quality. The update aims to streamline workflow and enhance patient experience by reducing rescans and improving diagnostic images.
2024-10
Diagnostic Imaging
Artifact Reduction Drives Technology Advances with Updated Version of Echelon Synergy MRI System | Diagnostic Imaging
Fujifilm Healthcare's Version 10 of the Echelon Synergy 1.5T MRI system focuses on artifact reduction with new technologies like Synergy DLR Clear and Synergy Vision, which uses AI and real-time tracking to mitigate motion and truncation artifacts. These advancements aim to improve image quality without extending scan times.
2024-10
AuntMinnie.com
Fujifilm launches version 10 of its Echelon Synergy MRI system - AuntMinnie
Fujifilm Healthcare Americas has released Version 10 (v10) for its Echelon Synergy 1.5-tesla MRI system, incorporating AI-driven features such as Synergy DLR Clear and Synergy Vision with StillShot to reduce motion artifacts and improve image clarity. The update also includes deep learning-enhanced AutoPose for various applications.
2024-10
Axis Imaging News
Fujifilm Launches AI Software for Echelon Synergy MRI - Axis Imaging News
Fujifilm Healthcare Americas Corp. launched Version 10 (v10) of its Echelon Synergy 1.5T MRI system, featuring AI-powered technologies like Synergy Vision with StillShot to reduce motion artifacts and DLR Clear to eliminate the u201cGibbsu201d artifact. These updates aim to enhance image quality, streamline workflow, and improve the patient experience.
2024-10
FUJIFILM Healthcare Americas Corporation
Fujifilm Launches New MRI System, ECHELON Synergy with Deep Learning Reconstruction Technology
FUJIFILM Healthcare Americas Corporation announced FDA 510(k) clearance for its new ECHELON Synergy 1.5 Tesla MRI system, which incorporates Synergy DLR, Fujifilm's AI-powered Deep Learning Reconstruction technology. This system is designed to enhance image sharpness and accelerate scan times, improving throughput and patient satisfaction.
2023-08
healthcare-in-europe.com
Fujifilm presents new MRI scanner at ECR 2024 - healthcare-in-europe.com
Fujifilm Healthcare Europe showcased its Echelon Synergy MRI system at ECR 2024, highlighting its 1.5 Tesla superconductive magnet and AI-powered features for enhanced image quality and scanning speed. The system emphasizes patient comfort with a wide bore and aims to improve workflow efficiency.
2024-02
Scribd
ECHELON Synergy MRI System Overview | PDF | Magnetic Resonance Imaging - Scribd
The ECHELON Synergy MRI system received FDA 510(k) clearance, determined to be substantially equivalent to the ECHELON OVAL V6.0A MRI system. This Class II magnetic resonance diagnostic device provides non-invasive imaging without ionizing radiation.
2022-11
accessdata.fda.gov
May 3, 2024 Fujifilm Healthcare Americas Corporation Chaitrali Kulkarni Sr. Regulatory Affairs Specialist 81 Hartwell Ave Suite - accessdata.fda.gov
The FDA issued a 510(k) clearance for the ECHELON Synergy System, confirming its intended use as an imaging device to provide physiological and clinical information non-invasively. The document details the system's capabilities in producing cross-sectional images of various body parts.
2024-05

Videos

Product demos, reviews, and walkthroughs for ECHELON Synergy MRI System.

View all on YouTube

Frequently Asked Questions

The ECHELON Synergy MRI system integrates AI-powered Deep Learning Reconstruction (DLR), including Synergy DLR Clear, to enhance image sharpness, reduce noise, and mitigate artifacts, significantly improving image quality and reducing scan times. Additionally, Synergy Vision with StillShot AI corrects motion-compromised data using real-time tracking, minimizing rescans, while AI-enhanced AutoPose and AutoExam One Touch automate workflows for increased efficiency.
The ECHELON Synergy MRI system, which includes its AI-powered Deep Learning Reconstruction technology, received 510(k) clearance from the U.S. Food and Drug Administration (FDA) in August 2023, classifying it as a Class II medical device. This regulatory approval confirms its safety and effectiveness for diagnostic imaging. While FDA clearance implies adherence to medical device data security standards, specific detailed protocols for patient data privacy like HIPAA or GDPR for the AI processing are not explicitly outlined in the provided information.
The ECHELON Synergy MRI System distinguishes itself with AI-powered Deep Learning Reconstruction (DLR) for superior image quality and faster scan times, alongside AI-driven motion correction and automated workflows. While other leading MRI manufacturers like GE, Siemens, and Philips offer their own advanced systems and imaging technologies, Fujifilm highlights the ECHELON Synergy's cost-effectiveness and low total cost of ownership as key competitive advantages.
The ECHELON Synergy MRI System is marketed as 'cost-effective' with an 'affordable total cost of ownership,' though specific pricing figures are not publicly disclosed in the search results. Notably, Fujifilm provides new AI features, such as Synergy DLR Clear and Synergy Vision with StillShot, as part of standard software updates (Version 10) to existing customers at no additional charge.
General MRI limitations, such as sensitivity to patient movement, susceptibility to artifacts from certain metal implants, and contraindications for specific patient groups, apply to the ECHELON Synergy. While its AI features like StillShot are designed to mitigate motion artifacts, the provided information does not explicitly detail potential biases of the AI algorithms themselves or specific mitigation strategies beyond their intended function to improve image quality.
The ECHELON Synergy MRI system's FDA 510(k) clearance in August 2023 indicates adherence to established medical device regulations and standards for safety and effectiveness. However, specific detailed protocols regarding patient data security, encryption, or compliance with regulations like HIPAA or GDPR for the AI processing within the system are not explicitly outlined in the provided search results.
Yes, the ECHELON Synergy MRI system is designed for interoperability with existing healthcare IT infrastructure. It implements IHE (Integrating the Healthcare Enterprise) integration profiles, specifically Scheduled Workflow (SWF) and Patient Information Reconciliation (PIR), which facilitates the integration of its images and workflow data with Picture Archiving and Communication Systems (PACS) and Electronic Medical Record (EMR) systems.

Related Tools

Surgical Reality Viewer
Surgical Reality
Oncology AI
Surgical Reality offers CE- and FDA-certified AI-powered 3D medical imaging and surgical planning software that transforms CT scans into patient-specific 3D models for thoracic surgery, enhancing precision in complex lung procedures.
Oxipit ChestLink
Oxipit (part of Sectra group)
Clinical Decision Support & Reference
Oxipit ChestLink is the world's first CE Class IIb-certified autonomous AI application for healthy chest X-ray reporting, capable of identifying normal studies with 99.9% sensitivity. It automates the reporting of normal chest X-rays, reducing radiologist workload and improving efficiency.
Cercare Medical Oncology Virtual Expert
Cercare Medical
Neurology AI
Cercare Medical's Oncology Virtual Expert is an AI-powered brain tumor segmentation module that provides fast, consistent, and semi-automated tumor analysis from standard MRI data, designed for on-premise deployment within existing clinical radiology workflows.
CARPL.ai
CARPL.ai
Developer Tools & APIs
CARPL.ai is a vendor-neutral Artificial Intelligence (AI) platform that allows radiologists to access, assess, and integrate radiology AI solutions in their clinical practice. It provides a single user interface, a single data channel, and a single procurement channel for the testing, deployment, and monitoring of AI solutions in clinical radiology workflows.
CoLumbo C-Spine
Smart Soft Healthcare AD
Clinical Decision Support & Reference
CoLumbo C-Spine is an AI-powered software that processes and analyzes cervical spine MRI exams, assisting clinicians in diagnosis and assessment.
SubtleHD-CT
Subtle Medical, Inc.
Radiology & Imaging AI
Subtle Medical's SubtleHD-CT is an AI software designed to enhance the quality and resolution of CT scans, reducing noise and improving image clarity. [7]

See all Radiology & Imaging AI tools →

Suggest an Edit → | Last Verified: 2026-04-18 | First Added: 2026-04-18
AI Tool Finder
AI-powered search. Results may not be comprehensive.