MAGNETOM Flow.Ace

by Siemens Healthineers  · Based in Germany → — The first virtually helium-free 1.5T MRI system with AI-powered workflows for human and veterinary radiology.
Radiology
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Regulatory Status Disclosed

Overview

MAGNETOM Flow.Ace by Siemens Healthineers is a next-generation 1.5 Tesla (T) magnetic resonance imaging (MRI) system designed for enhanced workflow, patient experience, and sustainability. It is notable as the company’s first 1.5T MRI platform to operate with a closed helium circuit, significantly reducing reliance on liquid helium to just 0.7 liters, compared to over 1,000 liters for conventional scanners. This is achieved through its innovative DryCool superconductive magnet technology, which also eliminates the need for a quench pipe, simplifying installation and reducing associated costs.

The system integrates advanced artificial intelligence (AI) for both workflow automation and image reconstruction. Its Deep Resolve technology enables accelerated image acquisition, reduces noise, and enhances the sharpness of small structures, leading to shorter scan times and improved image quality. This AI-driven approach streamlines patient registration, positioning, and scan initiation, allowing operators to manage these tasks directly at the patient’s side.

MAGNETOM Flow.Ace features a 60cm bore and is equipped with a new generation of intelligent and flexible BioMatrix Contour coils, facilitating easy positioning and adaptability to various anatomies for high-quality imaging. The system is versatile, intended for a broad spectrum of clinical and medical imaging applications, including whole-body studies, cardiac, oncology, neurology, and musculoskeletal applications. Uniquely, it is marketed for both general human radiology and veterinary radiology communities, with specialized coils available for both.

Committed to sustainability, the MAGNETOM Flow.Ace also features an Eco Power Mode, which automatically deactivates energy-intensive components when not in active use, leading to a reduction in annual energy consumption by more than 30% compared to previous generations of MR scanners.

Reviewed by Pouyan Golshani, MD — Interventional Radiologist

Key Features

  • 1.5 Tesla (T) MRI system
  • Virtually helium-free with DryCool superconductive magnet technology
  • AI-based software for simplified and guided workflows
  • Deep Resolve image reconstruction technology for higher resolution and shorter scan times
  • Reduced annual energy consumption by over 30% with Eco Power Mode
  • 60cm bore MRI scanner
  • No quench pipe required, simplifying installation
  • BioMatrix Contour coils for flexible patient positioning and high-quality imaging
  • Automated patient workflow
  • Suitable for both human and animal imaging

Use Cases

  • General radiology examinations
  • Veterinary radiology
  • Cardiac imaging
  • Oncology applications
  • Neurology imaging
  • Musculoskeletal imaging
  • Whole-body studies

What Physicians Need to Know

DICOM Support & Standards
As a modern MRI system, MAGNETOM Flow.Ace inherently supports DICOM for image transfer and storage, conforming to FDA recognized and international IEC, ISO, and NEMA standards.
PACS Integration Method
Standard PACS integration is supported, allowing for seamless transfer and archiving of MRI images via DICOM standards.
Reading Room Workflow Impact
AI-enabled workflows, including the myExam Companion function and BioMatrix Position Sensors, guide users through examinations, automate steps, and enable automated patient positioning for potentially faster exam setup. Deep Resolve AI assists in image reconstruction, reducing noise and improving image quality, which can lead to shorter scan times and improved diagnostic confidence.
AI Model Architecture (deep learning approach)
The system incorporates AI for automated workflow steps and image reconstruction. It features the Deep Resolve AI tool, which utilizes deep learning technology to speed up data collection, reduce image noise, and enhance the visibility of fine anatomical details.
Processing Speed (per study)
AI-based image reconstruction and automated workflows are designed to enable shorter scan times and accelerated image acquisition. While a general 'per study' speed is not specified, it is noted that cardiac MRI exams can be completed in under 30 minutes.
FDA Clearance Pathway (510k/De Novo)
MAGNETOM Flow.Ace received 510(k) clearance from the U.S. Food and Drug Administration (FDA) in June 2025 (K250436).
Supported Modalities (CT/MRI/X-ray/US)
MAGNETOM Flow.Ace is a 1.5 Tesla (T) Magnetic Resonance Imaging (MRI) system. It covers the entire range of MR applications for both general radiology and veterinary radiology.
Sensitivity & Specificity Data
Specific sensitivity and specificity data for the AI components or the overall system's diagnostic performance were not explicitly detailed in the available information.
Physician Tip

Physicians can expect enhanced image quality with reduced noise and improved detail thanks to Deep Resolve AI, potentially leading to more confident diagnoses. The automated workflows and shorter scan times may improve patient throughput and comfort, especially beneficial for anxious or less cooperative patients. The system's capability for a broad spectrum of MRI applications, including whole-body, cardiac, and oncology studies, offers versatility. Its availability for veterinary use also expands its utility in a mixed practice setting. The virtually helium-free DryCool technology contributes to environmental sustainability and potentially lower operational costs.

As a modern MRI system, MAGNETOM Flow.Ace integrates seamlessly into existing radiology IT infrastructures through DICOM for image communication and archiving with PACS. Its AI-driven features are embedded within the system's workflow (e.g., myExam Companion, Deep Resolve), suggesting a tightly integrated software and hardware solution. Compatibility with various MR coils, including BioMatrix Contour coils, ensures adaptability to diverse patient anatomies and clinical needs.

Details

Category Radiology & Imaging AI
Pricing Unknown
DeploymentOn-premise (MRI hardware)
Compliance
BAA Available Yes AI-estimated
HIPAA CompliantUnknown AI-estimated
FDA Status 1 AI-estimated

FDA 510(k) cleared (K250436) on June 26, 2025, as a 1.5 Tesla magnetic resonance imaging (MRI) system for both general human and veterinary radiology. The manufacturer is Siemens Shenzhen Magnetic Resonance, Ltd.
Integrations
EHR Not specified
Specialties Radiology

What the Web Says

The Siemens Healthineers MAGNETOM Flow.Ace is a 1.5T MRI scanner that has received FDA clearance. It is notable for being virtually helium-free, requiring only 0.7 liters of liquid helium for cooling compared to over 1,000 liters for conventional MRI scanners, which significantly reduces costs and environmental impact. The system also incorporates AI-enhanced image reconstruction (Deep Resolve) for faster scan times and improved image quality, and is designed for a wide range of human anatomies, with specific coils also available for veterinary applications.

Overall: Positive

Strengths

  • Virtually helium-free design, drastically reducing helium dependency and associated costs.
  • Reduced annual energy consumption by over 30% compared to previous generations, with an Eco Power Mode for further efficiency.
  • AI-enhanced Deep Resolve image reconstruction technology for shorter scan times and improved image quality, including sharper small structures and noise reduction.
  • Elimination of the quench pipe, simplifying installation requirements and reducing costs.
  • Compact size, contributing to easier installation and potentially lower infrastructure costs.
  • Versatile for both human and veterinary radiology, with a range of dedicated MR coils.

Limitations

  • No specific cons were found in the provided search results from physicians, healthcare IT, tech reviewers, Reddit, G2, or Capterra.
  • Limited independent reviews from physicians or tech reviewers are available, as most information comes from press releases and product descriptions.
  • No direct user opinions from platforms like Reddit, G2, or Capterra were found in the search results.

Based on reviews from: Cassling, Siemens Healthineers, AuntMinnie, Applied Radiology, Diagnostic Imaging, AccessGUDID - NIH, Innolitics, Scribd, Zazoom

Last updated: 2026-07-27

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Press & Coverage

Siemens Healthineers USA
Siemens Healthineers Receives FDA Clearance for Magnetom Flow.Ace, Company's First Helium-Free 1.5 Tesla Magnetic Resonance Scanner
Siemens Healthineers announced FDA clearance for Magnetom Flow.Ace, their first helium-free 1.5T MR scanner, which also marks their entry into the veterinary radiology market. The system features AI-based image reconstruction for faster, higher-quality scans and significantly reduces helium and energy consumption.
2025-06
Medical Product Outsourcing (MPO)
Siemens Healthineers Gains FDA Clearance for Magnetom Flow.Ace
Siemens Healthineers received FDA clearance for its Magnetom Flow.Ace, a 1.5T MR imaging platform with a closed helium circuit and no quench pipe, significantly reducing helium reliance. This system is also the first Siemens Healthineers MR scanner to be marketed for both general and veterinary radiology.
2025-07
Diagnostic Imaging
FDA Clears Virtually Helium-Free 1.5T MRI System from Siemens Healthineers
The FDA has granted 510(k) clearance for the Magnetom Flow.Ace MRI scanner, a virtually helium-free 1.5T system from Siemens Healthineers. It utilizes DryCool magnet technology, requiring only 0.7 liters of liquid helium over its lifetime, and incorporates AI-powered image reconstruction.
2025-06
AuntMinnie.com
Siemens Healthineers gets FDA nod for Magnetom Flow.Ace MRI scanner - AuntMinnie
Siemens Healthineers has received 510(k) clearance from the FDA for its Magnetom Flow.Ace MRI scanner, a 1.5-tesla platform with a closed helium circuit and no quench pipe. This system is also the first Siemens MRI scanner marketed for both human and veterinary radiology.
2025-06
Medical Device Network
Siemens Healthineers Magnetom Flow.Ace, US - Medical Device Network
The Magnetom Flow.Ace is a 1.5-Tesla MRI system from Siemens Healthineers that operates without a quench pipe and uses DryCool superconductive magnet design, requiring only 0.7 liters of liquid helium. It covers a broad spectrum of clinical imaging and reduces annual energy consumption by over 30%.
2026-01
DVM360
Innovative MRI system makes its US debut - DVM360
The Magnetom Flow.Ace, a 1.5T MRI platform from Siemens Healthineers, has been installed at the Animal Neurology Center in St. Louis, Missouri, marking its first US installation. This system is marketed for both veterinary and general radiology, uses minimal helium, and features AI-based image reconstruction.
2026-02
Siemens Healthineers USA
Vet Hospital Installs First Magnetom Flow.Ace Magnetic Resonance Scanner in U.S.
The Animal Neurology Center in St. Louis became the first U.S. healthcare institution to install the Magnetom Flow.Ace, Siemens Healthineers' helium-free 1.5T MR imaging platform. This system is designed for both veterinary and general radiology, featuring a closed helium circuit and no quench pipe.
2026-02
ImagePro Radiology
Next generation MRI - ImagePro Radiology
ImagePro Radiology in Johannesburg has acquired the Siemens MAGNETOM Flow.Ace MRI system, highlighting its AI-powered workflow automation, BioMatrix Technology, Deep Resolve AI Imaging for faster scans, and BioMatrix Contour Coils for patient comfort.
2025-10

Videos

Product demos, reviews, and walkthroughs for MAGNETOM Flow.Ace.

View all on YouTube

Frequently Asked Questions

The MAGNETOM Flow.Ace utilizes AI, including the myExam Companion function and Deep Resolve AI, to guide users through examinations, automate workflow steps, and improve image reconstruction. This results in shorter scan durations, reduced image noise, and enhanced visibility of fine anatomical details, ultimately streamlining the diagnostic process.
MAGNETOM Flow.Ace received clearance from the U.S. Food and Drug Administration (FDA) in June 2025. This clearance covers the entire system, including its integrated AI functionalities for image reconstruction and workflow automation, ensuring it meets established safety and efficacy standards for medical devices.
While specific details on data privacy protocols for MAGNETOM Flow.Ace's AI were not explicitly detailed, Siemens Healthineers, as a leading medical technology company, adheres to stringent regulatory compliance and data protection standards. Generally, AI in medical imaging systems processes anonymized or de-identified data to protect patient privacy while optimizing image acquisition and reconstruction.
A primary differentiator for MAGNETOM Flow.Ace is its virtually helium-free DryCool technology, requiring only 0.7 liters of liquid helium, significantly reducing operational costs and environmental impact compared to conventional MRI systems. Additionally, its AI-powered workflows and Deep Resolve image reconstruction technology aim to deliver faster scans with improved image quality and automated patient positioning.
The MAGNETOM Flow.Ace is designed for a highly attractive total cost of ownership due to its DryCool technology, which dramatically reduces helium dependency and associated refill costs. Furthermore, its compact size and elimination of a quench pipe can lower installation requirements and related expenses, alongside a reported reduction in annual energy consumption by over 30%.
The AI in MAGNETOM Flow.Ace primarily focuses on workflow automation, image reconstruction, and quality enhancement, acting as an assistant rather than a fully autonomous diagnostic tool. Physicians remain responsible for final image interpretation and clinical decision-making, as AI's role is to optimize data acquisition and presentation, not to replace expert medical judgment.
Siemens Healthineers is committed to continuous innovation, and as an upgradable platform, MAGNETOM Flow.Ace is expected to receive future software updates that could include new AI features and enhancements. These updates would aim to further improve imaging capabilities, workflow efficiency, and potentially expand clinical applications.

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Suggest an Edit → | Last Verified: 2026-04-20 | First Added: 2026-04-20
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