EVE Synergy; EVE Titan

The EVE-20M stimulation system provides electrical muscle stimulation and transcutaneous electrical nerve stimulation. Its indications include muscle-spasm relaxation, muscle re-education,…

Registry build 21.09.26

The EVE-20M stimulation system provides electrical muscle stimulation and transcutaneous electrical nerve stimulation. Its indications include muscle-spasm relaxation, muscle re-education, maintaining range of motion and management of chronic intractable, postsurgical or post-traumatic pain.

The system uses a Synergy handpiece and Pro handpieces with interchangeable tips. Synergy mode combines radiofrequency and low-frequency functions, while Pro mode uses the low-frequency function. A temperature sensor stops Synergy output when the skin surface exceeds 43 degrees Celsius.

Listed Item

1) EVE Synergy is also marketed under the brand name ‘EVE Titan’ with an updated logo design. 2) This device provides pain relief through RF (Radio Frequency), EMS (Electrical Muscle Stimulation), and TENS (Transcutaneous Electrical Nerve Stimulation) technologies. It should be noted that the device has radio frequency (RF Mode) indicated for relief of minor muscle aches and pain, relief of muscle spasm, temporary improvement of local blood circulation. This RF mode was previously reviewed by the FDA under K212253 and was cleared under regulation 21 CFR 878.4400 (Product code PBX). In the subject submission, there are no changes being proposed related to the RF Mode, and, hence, the review of the RF Mode is not within the scope of the subject 510(k) submission.

Muscle Stimulation Scope

Other EMS indications include prevention or retardation of disuse atrophy, increased local circulation and immediate postsurgical calf stimulation to prevent venous thrombosis. The device is intended for prescription use.

33manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (25), Beijing (3), Jiangsu (2). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code IPF
Manufacturer City Province Registered as Device types
JKH Health Co., Ltd. Dongguan Guangdong Contract manufacturer 22
Shenzhen Jie Zhong Lian Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 17
Beijing Winkonlaser Technology Limited Beijing Beijing Contract manufacturer 14
ATL Technology DG,Ltd. Dongguan Guangdong Contract manufacturer 14
Beijing Beautemax Technology Limited Beijing Beijing Contract manufacturer 13
Suzhou Fast ATM Electric Co., Ltd. Suzhou Jiangsu Contract manufacturer 2
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Beijing Choice Electronic Technololgy Co., Ltd. Beijing Beijing Repacker / relabeller 30
Hong Qiangxing (Shen Zhen) Electronics Limited Shenzhen Guangdong Contract manufacturer 19
Shenzhen Dongdixin Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 18
Guangzhou Xinbo Electronic Co., Ltd. Guangzhou Guangdong Contract manufacturer 18
Drtv Asia Ltd Panyu Guangzhou Guangdong Specification developer 16

Showing 12 of 33. All 33 manufacturers in China registered for Stimulator, Muscle, Powered

Record

Regulatory record for EVE Synergy; EVE Titan
Listed by Weero Co., Ltd., South Korea
FDA product code IPF
Device type Stimulator, Muscle, Powered
Device class Class 2
Regulation 21 CFR 890.5850
Establishment Manufacturer
510(k) K241433
Record published 2025-06-24
Record revised 2026-05-18 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for EVE Synergy; EVE Titan
Catalogue number Size Status
EVE-20M In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
QB1 Nmes System Motive Health, Inc. 69
MyndMove Myndtec Inc 44
GEM-Stim Gemore Technology Co., Ltd. 38
Chattanooga DJO, LLC 27
ReGrasp Rehabtronics, Inc. 19
Stimulation System Edan Instruments, Inc. 16
e-vive II Nmes System Motive Health, Inc. 16
L300 Go System Bioness Medical, Inc. 11
Motive Knee System Motive Health, Inc. 9
Ness H200® Wireless Hand Rehabilitation System Bioness Medical, Inc. 9
BodyMed Boxout, LLC 8
Everyway Everyway Medical Instruments Co., Ltd. 7

Showing 12 of 204. All products under Stimulator, Muscle, Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253542 2026-06-08
K241433 2025-06-04
K240992 2024-10-10

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