ECHELON Synergy

by Fujifilm Corporation  · Based in Japan → — Next Generation 1.5T MRI System with AI-Powered Deep Learning Reconstruction.
Neurology Orthopedics Radiology

Contact for pricing
Regulatory Status Disclosed

Overview

The FUJIFILM ECHELON Synergy is a state-of-the-art 1.5 Tesla (T) Magnetic Resonance Imaging (MRI) system designed and manufactured by FUJIFILM Healthcare. It incorporates proprietary Artificial Intelligence (AI) through Deep Learning Reconstruction (DLR) technology, known as Synergy DLR, to significantly enhance image clarity and expedite scanning times. [2, 7, 18, 22] The system received FDA 510(k) clearance in August 2023. [2, 7, 8, 18, 21]

ECHELON Synergy is built with patient comfort in mind, featuring a wide 70 cm bore and a 62 cm wide table that accommodates patients up to 550 lbs. [2, 7, 13, 16, 17, 18, 22] It also includes SoftSound™ gradient technology to reduce acoustic noise, improving the patient experience. [2, 7, 13, 16, 18, 22] The system’s design focuses on workflow efficiency with features like AutoExam One Touch operation, which automates patient positioning and scan initiation for brain and knee exams, and dual gantry monitors. [7, 13, 16, 18, 22]

Recent software updates, such as Version 10 (v10) released in October 2024, introduce further AI-powered enhancements like Synergy DLR Clear for artifact reduction and Synergy Vision with StillShot AI to mitigate motion artifacts, reducing the need for rescans. [3, 4, 5, 15] The system also features an anti-bacterial Hydro AG coating on high-contact surfaces to help reduce healthcare-associated infections (HAIs). [2, 7, 8, 18, 22]

Reviewed by Pouyan Golshani, MD — Interventional Radiologist

Key Features

  • AI-powered Synergy DLR (Deep Learning Reconstruction) for enhanced image clarity and faster scans
  • 1.5T Superconducting Magnet with 70 cm wide bore for patient comfort
  • SoftSoundu2122 gradient technology to reduce acoustic noise
  • Hydro AG antibacterial coating on high-touch surfaces to reduce HAIs
  • AutoExam One Touch operation for automated workflow and faster exam times
  • Synergy Vision with StillShot AI for real-time motion artifact mitigation
  • DLR Clear, an AI-based algorithm for truncation artifact reduction
  • AutoPose for automatic slice selection in breast, hip, and spine applications
  • IP-RAPID and IterativeRAPID for accelerated imaging across anatomical regions
  • FlexFit RF coil technology for flexible and comfortable patient positioning

Use Cases

  • High-resolution imaging of the head, body, spine, and extremities
  • Neuroimaging with reduced scan times and motion artifacts
  • Orthopedic imaging with improved clarity and speed
  • Breast imaging with Deep Learning enhanced AutoPose
  • Enhancing patient comfort and reducing anxiety during MRI exams
  • Streamlining workflow and increasing patient throughput in imaging centers

What Physicians Need to Know

DICOM Support & Standards
The ECHELON Synergy MRI system supports the DICOM 3.0 standard and TCP/IP Network Communication. A DICOM Conformance Statement for ECHELON Synergy V9.0 or later is available.
Reading Room Workflow Impact
The system streamlines workflow and reduces examination times through features like AutoExam One Touch for brain and knee exams, AutoPose for breast, hip, spine, and whole-body applications, AutoSet, and AutoStart, which automate patient positioning and scan initiation. Synergy DLR and AI-powered StillShot for motion correction further enhance efficiency by reducing manual steps and the need for rescans.
AI Model Architecture (deep learning approach)
ECHELON Synergy utilizes Fujifilm's proprietary Deep Learning Reconstruction (DLR) technology, known as Synergy DLR, which is powered by artificial intelligence. It also incorporates AI-driven features like StillShot for real-time motion correction and DLR Clear for truncation artifact reduction.
Processing Speed (per study)
Synergy DLR technology is reported to reduce scan time by 50% compared to previous generation MRI systems. Brain exams can be completed in as little as five minutes. Studies suggest AI reconstruction can deliver scans four times faster than standard methods.
FDA Clearance Pathway (510k/De Novo)
The ECHELON Synergy MRI system received 510(k) clearance from the U.S. Food and Drug Administration (FDA) in August 2023.
Supported Modalities (CT/MRI/X-ray/US)
ECHELON Synergy is specifically a 1.5 Tesla Magnetic Resonance Imaging (MRI) system.
Sensitivity & Specificity Data
While specific sensitivity and specificity data for the AI components are not explicitly provided, clinical image testing for related DLR technology demonstrated superior artifact reduction, SNR, image sharpness, and lesion conspicuity, with statistically significant differences (p<0.05) and clinically acceptable image quality.
RSNA/ACR Validation
Fujifilm showcases its medical technology advancements at RSNA conferences. The company also supports sites in achieving ACR, IAC, and TJC accreditations by providing an Accreditation Guidebook and assistance with phantom data collection.
Physician Tip

For radiologists, ECHELON Synergy's AI-powered Deep Learning Reconstruction (DLR) and motion correction (StillShot) can lead to sharper images and fewer motion artifacts, potentially improving diagnostic confidence and reducing the need for repeat scans. The automated workflow features (AutoExam One Touch, AutoPose) can significantly reduce technologist workload and scan times, enhancing patient throughput and overall department efficiency. Physicians should leverage the faster acquisition times to potentially expand MRI access and reduce patient wait times, while also appreciating the improved patient comfort features that can lead to better image quality due to reduced patient anxiety and movement.

ECHELON Synergy, as an MRI system, natively supports DICOM 3.0 for image transfer. Its integration into a broader healthcare IT ecosystem is facilitated by Fujifilm's enterprise imaging solutions like Synapse PACS, which can embed AI and advanced visualization directly into the reading workflow. This allows for seamless image processing, management, and review within existing PACS environments, optimizing the flow of AI-enhanced MRI data to radiologists.

Details

Category Radiology & Imaging AI
Pricing Contact for pricing
  • Pricing information is not publicly available; contact Fujifilm Healthcare Americas Corporation for a quote
  • [6, 17, 22]
DeploymentOn-premise (MRI system installation)
Compliance
BAA AvailableUnknown AI-estimated
HIPAA CompliantUnknown AI-estimated
FDA Status 1 AI-estimated

The ECHELON Synergy 1.5T MRI system received FDA 510(k) clearance in August 2023 (initial clearance K241429). [2, 7, 8, 18, 21, 27] Subsequent 510(k) submissions, such as K251386 (dated September 17, 2025), pertain to modifications or software updates to the cleared device. [27, 29]

Integrations
EHR Not specified
Specialties Neurology, Orthopedics, Radiology

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Clinical Value
Ease of Use
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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, introducing AI-powered enhancements like Synergy DLR Clear and Synergy Vision with StillShot to improve image quality and workflow. The software aims to address issues like patient motion and truncation artifacts, with features like automated scanning processes.
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 utilizes proprietary Deep Learning Reconstruction (DLR) technology powered by AI for enhanced image sharpness and faster scans. The system also features a wide bore and automated workflow for improved patient comfort and efficiency.
2023-08
Medical Device Network
Fujifilm's Echelon Synergy Magnetic Resonance Imaging (MRI) System, USA
Fujifilm's Echelon Synergy MRI system, a 1.5T system with AI-powered Synergy DLR, received 510(k) clearance in August 2023 and was launched in Europe and India in early 2024. The system is designed for enhanced patient comfort with a wide bore and features automated workflow capabilities.
2024-04
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 software, incorporating AI-powered technologies like Synergy Vision with StillShot to reduce motion artifacts and DLR Clear to address truncation artifacts. These updates aim to improve image clarity, streamline workflow, and enhance the patient experience.
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 through Synergy Vision and StillShot AI, which mitigate motion artifacts. The update also includes DLR Clear, an AI-powered algorithm to address truncation artifacts without extending scan times.
2024-10
interhospi.com
FUJIFILM Healthcare Europe unveils ECHELON Synergy MRI scanner
FUJIFILM Healthcare Europe launched the ECHELON Synergy MRI scanner at ECR in Vienna, highlighting its AI-powered deep learning reconstruction for efficient, high-performance imaging and patient comfort. The 1.5 Tesla system features a 70 cm wide bore and automated scanning controls to improve workflow and patient experience.
2026-06
RAD Magazine
Echelon Synergy ZeroHelium offering enhanced energy efficiency is launched in the UK - RAD Magazine - The voice of medical imaging and clinical oncology
Fujifilm launched the Echelon Synergy ZeroHelium in the UK, an MRI technology that eliminates the need for liquid helium, promoting sustainability and flexible installation. This wide-bore system enhances patient comfort and features IQ-Retouch for artifact reduction and AutoExam for automated workflow.
2025-11
accessdata.fda.gov (FDA)
FUJIFILM Healthcare Americas Co 510(k) Premarket Notification
This FDA 510(k) premarket notification details the ECHELON Synergy System as an imaging device intended to provide physiological and clinical information non-invasively. It describes the MR system's ability to produce cross-sectional images of the head, body, or extremities, reflecting the spatial distribution of protons.
2025-09

Videos

Product demos, reviews, and walkthroughs for ECHELON Synergy.

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Frequently Asked Questions

ECHELON Synergy utilizes AI-powered Deep Learning Reconstruction (Synergy DLR) to improve image clarity and significantly reduce scan times, with brain exams taking as little as five minutes. It also incorporates AI tools like StillShot for real-time motion correction and AutoPose for automated patient positioning, streamlining workflow and reducing the need for rescans.
The ECHELON Synergy 1.5T MRI system, including its AI-powered Synergy DLR technology, received FDA 510(k) clearance in August 2023. This clearance indicates that the device is substantially equivalent to a legally marketed predicate device and meets established safety and effectiveness standards.
As with all MRI systems, ECHELON Synergy has limitations, including sensitivity to patient movement, although its AI-powered StillShot aims to mitigate this. It is also susceptible to artifacts from certain types of metal and has inherent contraindications for specific patient groups, consistent with general MRI technology.
ECHELON Synergy is positioned as a high-performance, cost-effective 1.5T MRI system that offers advanced AI-powered Deep Learning Reconstruction (DLR) for improved image quality and faster scans. Its features, such as reduced scan times and enhanced patient comfort through a wide bore and quiet technology, are designed to provide competitive advantages in the 1.5T MRI market.
ECHELON Synergy is described as a cost-effective system with an affordable total cost of ownership, offering flexible siting options and low power consumption. Fujifilm also provides software updates, such as the Version 10 features, to current customers at no additional charge, contributing to long-term value.
As an FDA-cleared medical device, ECHELON Synergy is designed to comply with relevant regulations, including the Quality System (QS) regulation (21 CFR Part 820) for device manufacturing and DICOM 3.0 for image management. These standards encompass protocols for secure data handling and interoperability.
Clinical testing has confirmed the efficacy of the ECHELON Synergy system, with safety studies demonstrating that its Deep Learning Reconstruction (DLR) enhances image quality compared to conventional methods. Studies also indicate that AI reconstruction can deliver scans significantly faster, potentially expanding MRI access and improving patient throughput.

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Suggest an Edit → | Last Verified: 2026-04-18 | First Added: 2026-04-18
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