Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029924973

FEI Number

3029924973

Entity Name

SHENZHEN SINREL TECH LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

1st Floor, Building 6, No.27, Yongnan Road,Shajing Street, Baoan District, Shenzhen Guangdong 518103, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SHENZHEN SINREL TECH LTD (Owner Number: 10089019)

Owner / Operator Contact Address

1st Floor, Building 6, No.27, Yongnan Road,Shajing Street, Baoan District, Shenzhen, CN-GD 518103, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K220005

PMA Number

N/A

All Registered Proprietary Names

TENS & PMS Unit, YF1503, YF1503X, YF1504, YF1504V, YF1508C, YF1510, YF1511, YF1512, YF1513 YF1505, YF1506, YF1556, OX1503 TENS XS PRO YF1566

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2023-10-29
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2023-10-29

Official Correspondent

Lianghao Li

US Agent Details

Terry Chai Email: Terry.Chai.Nj@Hotmail.Com Phone: (908) 6361278

Related Public Records

Same Entity

SHENZHEN SINREL TECH LTD

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K221200	Xbody Hungary Kft.	XBody Go USA, XBody Pro USA	2023-01-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029924973. Last updated year: 2026. Please use registration number 3029924973 when referencing this establishment in official correspondence.