Roovjoy

It is used for temporary relief of pain associated with sore and aching muscles in the neck, shoulder, back, joint, hip,hand, abdomen, foot, upper extremities (arm) and lower extremities…

Registry build 21.09.26

It is used for temporary relief of pain associated with sore and aching muscles in the neck, shoulder, back, joint, hip,hand, abdomen, foot, upper extremities (arm) and lower extremities (leg) due to strain from exercise or normal household work activities.

57manufacturers in China registered for this device type
22catalogue numbers in this listing
3510(k) clearances naming this product code

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 Roovjoy
Listed by Shenzhen Roundwhale Technology 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 Contract manufacturer, Manufacturer
510(k) K180956
Record published 2018-07-16
Record revised 2023-06-02 (version 11)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Over the counter Yes
Label carries lot or batch number, expiry date, manufacturing date
Packaging Pack of 50, box of 50, pack of 32, pack of 20
Distribution end date 2020-05-28

Catalogue Numbers

Catalogue numbers for Roovjoy
Catalogue number Size Status
R-T1 In distribution
M100B In distribution
R-C101C In distribution
R-C4A In distribution
MINI TENS COMBO In distribution
R-C6 In distribution
M101A In distribution
R-C5 In distribution
R-C101A In distribution
R-C1 In distribution
M100A In distribution
R-C101K In distribution
TENS3500 In distribution
F100 In distribution
M101B In distribution
R-C101G In distribution
M102A In distribution
R-C101N In distribution
R-C101F In distribution
R-C101D In distribution
R-C1 Withdrawn
R-T1 Withdrawn

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
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
iSTIM Everyway Medical Instruments Co., Ltd. 9

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
K231423 2024-01-22
K192087 2019-11-01
K180956 2018-06-07

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