Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010485091

FEI Number

3010485091

Entity Name

Shenzhen Minghuangda Electronics Co.,LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Floor 6, Building A, Taixinglong Industrial Park, Hezhou Village, Xixiang Town, Baoan District, Shenzhen Guangdong 518100, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Shenzhen Minghuangda Electronics Co.,LTD (Owner Number: 10061384)

Owner / Operator Contact Address

Floor 6, Building A, Taixinglong Industrial Park, Hezhou Village, Xixiang Town, Baoan District, Shenzhen, CN-GD 518100, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K241678

PMA Number

N/A

All Registered Proprietary Names

MHD TENS, MH-1080, MH-1083, MH-1085, MH-1088,MH-100B EMS Muscle Stimulator, MH-1038, MH-1048 foot massager (MH-1019) EMS Muscle Stimulator, MH-100B Foot massager, MH-1019 TENS & EMS Stimulator, MHD-1083, MH-1080, MH-1083, MH-1087, MH-1036

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	2019-10-14
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2019-10-14
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2024-09-23
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2024-09-23

Official Correspondent

Ada Zhang

US Agent Details

Mark Gordon Email: Mark.W.Gordon@outlook.com Phone: (920) 6019045

Related Public Records

Same Entity

Shenzhen Minghuangda Electronics Co.,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 3010485091. Last updated year: 2026. Please use registration number 3010485091 when referencing this establishment in official correspondence.