Everyway

Electrode conductive pad A small, non-sterile device designed to facilitate electrical conduction between an electrical stimulation electrode and the skin. It is typically contoured to fit…

Registry build 21.09.26

Electrode conductive pad A small, non-sterile device designed to facilitate electrical conduction between an electrical stimulation electrode and the skin. It is typically contoured to fit on a particular type of electrode and is made of an absorbent material (e.g., felt) that may be soaked in a conduction fluid.

47manufacturers in China registered for this device type
35catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (29), Jiangsu (4), Zhejiang (4). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GXY
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Shenzhen Konmed Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
China Qingdao Bright Medical Manufacturing Co., Ltd. Qingdao Shandong Contract manufacturer 8
Pine Moon Electronics Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Top-rank Health Care Co., Ltd. Shaoxing Zhejiang Contract manufacturer 7
Omron (Dalian) Co., Ltd. (Plant 1) Dalian Liaoning Contract manufacturer 7
Shenzhen Zifound Infonet Technology Co., Ltd. Shenzhen, Guandong Guangdong Contract manufacturer 2
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Beijing Choice Electronic Technololgy Co., Ltd. Beijing Beijing Repacker / relabeller 30
Taizhou Chenguang Import AND Export Trading Co., Ltd. Taizhou Jiangsu Exporter 25

Showing 12 of 47. All 47 manufacturers in China registered for Electrode, Cutaneous

Record

Regulatory record for Everyway
Listed by Everyway Medical Instruments Co., Ltd., Taiwan
FDA product code GXY
Device type Electrode, Cutaneous
Device class Class 2
Regulation 21 CFR 882.1320
Establishment Manufacturer
510(k) K173186
Record published 2023-08-30
Record revised 2025-12-08 (version 3)

Specifications

Specifications
MRI safety MR Safe
Prescription Prescription only
Over the counter Yes
Latex Labelled latex-free
Label carries serial number

Catalogue Numbers

Catalogue numbers for Everyway
Catalogue number Size Status
SG50D In distribution
TKF5050 In distribution
TKF4080 In distribution
TKF4060V In distribution
SG60147 In distribution
TKF5050 In distribution
KF50100 In distribution
AF40350 In distribution
TKF50100V In distribution
KF4060V In distribution
KF4080 In distribution
KF50D In distribution
SG5075 In distribution
S80120 In distribution
SG4368 In distribution
SG5795 In distribution
AF100152 In distribution
TKF4040 In distribution
AF5050 In distribution
SG5050 In distribution
KF50100V In distribution
SKB5050 In distribution
SG4040 In distribution
SG7090 In distribution
AF4040 In distribution
KF4040 In distribution
TKF50100 In distribution
S55105 In distribution
TKF75D In distribution
SG75D In distribution
KF75D In distribution
TKF50100V In distribution
TKF50D In distribution
SG50100 In distribution
KF5050 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Rhythmlink® Rhythmlink International, LLC 455
waveguard Eemagine Medical Imaging Solutions Gmbh 166
Espire Elbow Hybrid College Park Industries 138
Technomed Europe Technomed Engineering B.V. 126
Cadwell Technomed Engineering B.V. 111
The Electrode Store Impulse Technology LLC 109
Electrode, Cutaneous Gmdasz Manufacturing Co., Ltd. 99
Auvon Shenzhen Yuwen E-Commerce Co., Ltd. 93
AdvanTrode Pepin Manufacturing, Inc. 78
Uni-Patch Cardinal Health 77
Alpha WillowWood Global LLC 68
Espire Elbow Pro College Park Industries 67

Showing 12 of 1,006. All products under Electrode, Cutaneous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K173186 2018-02-28
K103719 2011-08-24
K083302 2009-08-03
K012463 2002-02-05

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