Transcutaneous Electrical Nerve Stimulator

The ST-304 Transcutaneous Electrical Nerve Stimulator is a wearable home-use device for adults with sore or aching muscles at the back of the neck. It provides temporary pain relief for…

Registry build 21.09.26

The ST-304 Transcutaneous Electrical Nerve Stimulator is a wearable home-use device for adults with sore or aching muscles at the back of the neck. It provides temporary pain relief for strain associated with exercise or normal household and work activities. It is available over the counter.

Two fixed titanium electrode pads deliver low-frequency electrical pulses through intact neck skin. Users select either of two stimulation modes and adjust intensity through 15 levels. Conductive gel is applied to the pads before use. The default session lasts ten minutes.

Heat and Power

A separate heating mode provides a warming temperature of 32 to 38 degrees Celsius and can run alone or with stimulation. A rechargeable 3.7 V lithium battery powers the unit. The device cannot be used while charging, and manual buttons control power, mode, heat and intensity.

57manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (40), Beijing (2), Tianjin (2). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NUH
Manufacturer City Province Registered as Device types
Andon Health Co., Ltd. Tianjin Tianjin Contract manufacturer 22
JKH Health Co., Ltd. Dongguan Guangdong Contract manufacturer 22
Shenzhen Jie Zhong Lian Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 17
Dongguan Quanding Medical Supplies Co., Ltd. Dongguan Guangdong Contract manufacturer 14
Shenzhen Yicai Health Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
Omron (Dalian) Co., Ltd. (Plant 1) Dalian Liaoning Contract manufacturer 7
Shenzhen Jiantuo Electronics Co., Ltd. Shenzhen Guangdong Contract manufacturer 4
Ebulent Optronics (Shenzhen) Ltd Shenzhen Guangdong Contract manufacturer 4
Ansion Technology (GuangDong) Co., Ltd. Dongguan Guangdong Contract manufacturer 3
Shenzhen Life-King Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 2
Beijing Choice Electronic Technololgy Co., Ltd. Beijing Beijing Repacker / relabeller 30
Beijing Spiritlaser Science & Technology Co., Ltd. Beijing Beijing Contract manufacturer 21

Showing 12 of 57. All 57 manufacturers in China registered for Stimulator, Nerve, Transcutaneous, Over-The-Counter

Record

Regulatory record for Transcutaneous Electrical Nerve Stimulator
Listed by Shenzhen Future Electronic Co., Ltd., China
FDA product code NUH
Device type Stimulator, Nerve, Transcutaneous, Over-The-Counter
Device class Class 2
Regulation 21 CFR 882.5890
Establishment Manufacturer, Exporter
510(k) K221092
Record published 2022-09-30
Record revised 2023-06-02 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Transcutaneous Electrical Nerve Stimulator
Catalogue number Size Status
ST-304 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Auvon Shenzhen Yuwen E-Commerce Co., Ltd. 114
Transcutaneous Electrical Nerve Stimulators Shenzhen Kentro Medical Electronics Co., Ltd. 36
Everyway Everyway Medical Instruments Co., Ltd. 28
Avcoo ADP Health Limited 23
Roovjoy Shenzhen Roundwhale Technology Co., Ltd. 22
Auvon Shenzhen As-Tec Technology Co., Ltd. 17
Transcutaneous Electrical Nerve Stimulator Shenzhen Kentro Medical Electronics Co., Ltd. 15
Sinrel Shenzhen Sinrel Tech Ltd 13
Electronic Stimulator Shenzhen Leqing Medical Instrument Co., Ltd. 13
kentro Shenzhen Kentro Medical Electronics Co., Ltd. 12
Avazzia Avazzia, Inc. 11
Beurer Beurer North America, L.P. 10

Showing 12 of 230. All products under Stimulator, Nerve, Transcutaneous, Over-The-Counter

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K221092 2022-09-13

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