Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012500350

FEI Number

3012500350

Entity Name

HONGKONG SHARED DREAM ENTERPRISE LIMITED

City/State/Country

Kowloon, HK

Establishment Address

19H MAXGRAND PLAZA, NO.3 TAI YAU STREET SAN PO KONG, Kowloon 999077, HK

Establishment Type(s)

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

Owner / Operator

HONGKONG SHARED DREAM ENTERPRISE LIMITED (Owner Number: 10060705)

Owner / Operator Contact Address

19H MAXGRAND PLAZA, NO.3 TAI YAU STREET SAN PO KONG, Kowloon, HK-NOTA 999077, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K121719

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

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	2021-01-20
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2021-01-20
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2019-06-13
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2019-06-13

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

HONGKONG SHARED DREAM ENTERPRISE LIMITED

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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3011562129	MIRAE MEDI&TECH CO., LTD.	Cheonan-si Chungnam, KR
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012500350. Last updated year: 2026. Please use registration number 3012500350 when referencing this establishment in official correspondence.