Echelon Synergy

Echelon Synergy is an MRI system using a 1.5 tesla superconducting magnet in a gantry. Radiofrequency excitation and magnetic field gradients generate signals that are reconstructed into…

Registry build 21.09.26

Echelon Synergy is an MRI system using a 1.5 tesla superconducting magnet in a gantry. Radiofrequency excitation and magnetic field gradients generate signals that are reconstructed into anatomical images.

Different pulse sequences emphasize properties including T1 and T2 relaxation, proton density and molecular diffusion. These properties contribute to image contrast, and the system also supports spectroscopy.

System Configurations

This configuration adds an alternative ZeroHelium superconducting magnet and a dockable patient table, with a corresponding Spine Coil B option. Application software is Version V11.0A.

12manufacturers in China registered for this device type
2catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (3), Beijing (2), Guangdong (2). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LNH
Manufacturer City Province Registered as Device types
Shanghai Chenguang Medical Technologies Co., Ltd. Shanghai Shanghai Contract manufacturer 2
GE Healthcare (China) Co., Ltd. Beijing Beijing Specification developer 22
Shanghai United Imaging Healthcare Co., Ltd. Shanghai Shanghai Manufacturer 12
Siemens Shenzhen Magnetic Resonance Ltd. Shenzhen Guangdong Contract manufacturer 8
GE Healthcare (Tianjin) Company Limited Tianjin Tianjin Specification developer 5
GE Healthcare (China) Co., Ltd. – Tianjin Tianjin Tianjin Specification developer 3
Shenzhen RF Tech Co., Ltd. Shenzhen Guangdong Complaint-file establishment 2
Shanghai Chenshi Medical Instruments Co., Ltd. Shanghai Shanghai Exporter 2
MRI Division, Beijing Wandong Medical Technology Co., Ltd. Beijing Beijing Manufacturer 1
Jiangsu Magspin Instrument Co., Ltd. Kunshan Jiangsu Manufacturer 1
Xingaoyi Medical Equipment Co., Ltd. Yuyao Zhejiang Manufacturer 1
Sino Canada Health Engineering Research Institute (Hefei) Ltd. (Scheri) Hefei Anhui Complaint-file establishment 1

Record

Regulatory record for Echelon Synergy
Listed by Fujifilm Corporation, Japan
FDA product code LNH
Device type System, Nuclear Magnetic Resonance Imaging
Device class Class 2
Regulation 21 CFR 892.1000
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K251386
Record published 2024-09-11
Record revised 2025-05-13 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment temperature 20 to 24 °C; Handling environment humidity 45 to 60 % RH; Storage environment temperature -15 to 55 °C; Storage environment humidity 10 to 95 % RH; Storage environment atmospheric pressure 70 to 106 KiloPascal

Catalogue Numbers

Catalogue numbers for Echelon Synergy
Catalogue number Size Status
ECHELON Synergy In distribution
MR-TSP-156B In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Ingenia Philips Medical Systems Nederland B.V. 72
System, Nuclear Magnetic Resonance Imaging GE Medical Systems, L.L.C. 40
System, Nuclear Magnetic Resonance Imaging Medtronic Navigation, Inc. 23
Uni-frame® Thermoplastic Medtec LLC 19
Positioning Cushion Medtec LLC 18
Posicast® Thermoplastic Medtec LLC 18
System, Nuclear Magnetic Resonance Imaging GE Healthcare (Tianjin) Company Limited 16
Invivo Philips DS North America LLC 15
Type-S™ Thermoplastic Medtec LLC 14
Aperto Lucent Fujifilm Corporation 13
MRI Integral “T” with Check Valve for Medrad® Spectris MR Injector Bayer Medical Care Inc. 11
PPG Finger Band IVY Biomedical Systems, Inc. 11

Showing 12 of 478. All products under System, Nuclear Magnetic Resonance Imaging

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253862 2026-04-06
K251386 2025-09-17
K241429 2024-08-13
K240571 2024-04-12
K223426 2023-07-13
K221619 2023-01-26

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P860010 1988-06-12 INSTRUMENTARIUM ULF MR IMAGING SYSTEM Palomex Instrumentarium Corp.
P860062 1988-05-25 RESONEX RX4000{TM} MAGNETIC RESONANCE IMAGING SYST Resonex, Inc.
P850043 1987-12-30 MAGNISCAN 5000 MRI SYSTEM Thomson-Cgr Medical Corp.
P830074 1987-11-25 GE SIGNA MAGNETIC RESONANCE DIAGNOSTIC IMAGING SYS General Electric Co.
P840063 1987-08-11 GYROSCAN(TM) Philips Medical Systems Technologies Ltd
P840007 1987-04-02 GYREX, MODELS S3500 & S5000 Elscint, Inc.
P830076 1986-10-08 FONAR NMR WHOLE BODY SCANNER BETA 3000 Fonar Corp.
P830052 1986-05-28 NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000 Philips Medical Systems (Cleveland), Inc.
P830051 1986-04-30 TESLACON(TM) NMR IMAGING SYSTEM Technicare Corp.
P830053 1985-12-18 DIASONICS NMR IMAGING SYSTEM Diasonics, Inc.
P830081 1985-06-06 MAGNETOM Siemens Healthcare Limited

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer