MAGNETOM Flow.Neo
Overview
The MAGNETOM Flow.Neo is part of the MAGNETOM Flow. Platform, a next-generation 1.5 Tesla (T) Magnetic Resonance Imaging (MRI) system developed by Siemens Healthineers. This platform is designed to deliver unparalleled imaging care through a game-changing new workflow, ushering in a sustainable era of AI-powered and virtually helium-independent MRI.
Key innovations include its DryCool technology, which significantly reduces the need for liquid helium from over 1,000 liters to just 0.7 liters, eliminating the need for helium refills and a quench pipe. This contributes to resource conservation, reduced costs, and simplified installation. The system also features advanced energy-saving modes, such as Eco Power Mode Pro, which intelligently regulates cooling performance based on scanner load, leading to substantial annual energy savings.
The MAGNETOM Flow. Platform integrates artificial intelligence (AI) to enhance various aspects of MRI. Its Deep Resolve AI-powered algorithms are at the forefront of MRI acceleration, enabling faster acquisition times, improved image quality, and extraordinary clarity, now expanded to 3D imaging. AI also supports automated workflows, simplifying complex examinations and increasing productivity in clinical routines. Features like myExam Assist and myExam Autopilot provide adaptive, automated strategies, and myExam Implant Suite offers straightforward setup for safely scanning patients with implants.
Designed with patient comfort in mind, the platform offers a 70 cm bore size and flexible BioMatrix Contour coils that adapt to patient anatomy. New bone conduction audio technology in head and neck coils aims to improve patient interaction and reduce anxiety during examinations. The MAGNETOM Flow. Platform is a scalable and upgradeable solution, allowing healthcare facilities to adapt the system to evolving clinical needs and protecting their investment by enabling in-generation upgrades without magnet removal.
Reviewed by Pouyan Golshani, MD — Interventional Radiologist
Key Features
- AI-powered Deep Resolve image reconstruction (2D and 3D)
- Virtually helium-free DryCool magnet technology (0.7 liters)
- Eco Power Mode Pro for reduced energy consumption
- Automated workflows (myExam Assist, myExam Autopilot)
- Enhanced patient comfort (70 cm bore, BioMatrix Contour coils, ComfortSound audio)
- Scalable and upgradeable MRI platform
- Compact footprint and no quench pipe for easier installation
- High-density BioMatrix Contour coils for flexible patient coverage
- Support for interventional procedures with MR compatible devices
- Designed for high patient throughput and workflow efficiency
Use Cases
- Routine diagnostic MRI imaging
- Advanced imaging for neurology, cardiac, and oncology
- Musculoskeletal imaging
- Whole-body imaging and screening
- Interventional MRI procedures
- Veterinary MRI applications (for the Flow. Platform)
What Physicians Need to Know
For physicians, MAGNETOM Flow.Neo offers significantly faster scan times with improved image quality and sharpness, thanks to Deep Resolve AI. This can lead to higher patient throughput and reduced motion artifacts, especially beneficial for challenging cases like cardiac or pediatric imaging. The automated workflows (myExam Assist, myExam Autopilot) simplify complex examinations, potentially reducing variability and enhancing diagnostic consistency. The ability to perform patient registration and scan initiation at the patient's side can also improve the patient experience and overall workflow efficiency.
MAGNETOM Flow.Neo is designed for seamless integration into existing hospital IT environments, particularly with PACS, ensuring efficient access, storage, and sharing of high-quality MRI data. Its adherence to DICOM standards facilitates interoperability with various imaging and information systems. The platform's upgradability also ensures future-proof growth and adaptability to evolving healthcare demands and technological advancements.
Details
| Category | Radiology & Imaging AI |
| Pricing |
Contact for pricing
|
| Deployment | On-premise (integrated MRI system) |
| Compliance | |
| BAA Available | Unknown AI-estimated |
| HIPAA Compliant | Unknown AI-estimated |
| FDA Status |
1 AI-estimated The MAGNETOM Flow.Neo is part of the MAGNETOM Flow. Platform, which received FDA 510(k) clearance (K252838) as a magnetic resonance diagnostic device (MRDD) on December 19, 2025. It is indicated for producing transverse, sagittal, coronal, and oblique cross-sectional images, spectroscopic images, and/or spectra of the head, body, or extremities, providing information that may assist in diagnosis. |
| Integrations | |
| EHR | Not specified |
| Specialties | Interventional Radiology, Radiology |
What the Web Says
The Siemens Healthineers MAGNETOM Flow.Neo is a 1.5T MRI platform that has received FDA clearance. It is designed to reduce helium dependency and energy consumption, utilizing a closed helium circuit and DryCool technology that requires only 0.7 liters of liquid helium for cooling, significantly less than conventional MRI scanners. The system also incorporates AI-based image reconstruction and automated workflow tools to enhance image quality and shorten scan times.
Overall: MixedStrengths
- Reduced helium dependency and consumption (0.7 liters of liquid helium).
- Lower annual energy consumption (up to 56% reduction compared to previous generations).
- AI-based image reconstruction (Deep Resolve 2D and 3D) for improved image quality and shorter scan times.
- Automated workflow tools (myExam Assist, myExam Autopilot, myExam Implant Suite) for simplified and faster exams.
- Elimination of the quench pipe, leading to reduced installation requirements and costs.
- 70cm bore for increased patient comfort and broader application range.
Limitations
- One Reddit user reported frequent issues with a related Siemens MRI system (MAGNETOM Altea), though this may not directly apply to Flow.Neo.
- No clinical trials were conducted; evidence consists of bench testing, software verification, and sample clinical images.
- Specific pricing and deployment information is not publicly available.
- Limited independent reviews from physicians, healthcare IT, or tech reviewers are currently available.
- No reviews found on G2 or Capterra.
- The system was cleared by the FDA in December 2025, so long-term user experience may be limited.
Based on reviews from: AuntMinnie, Diagnostic Imaging, Applied Radiology, FDA 510(k) (Innolitics), AccessGUDID - NIH, Reddit, Radiology AI Tools Directory
Last updated: 2026-07-21
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