HONG KONG ETECH GROUPS LIMITED

FDA Device Registration & Listing · HONGKONG, HK · Registration 3022929665

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3022929665
FEI Number
3022929665
Entity Name
HONG KONG ETECH GROUPS LIMITED
City/State/Country
HONGKONG, HK
Establishment Address
ROOM 747,7/F,STAR HOUSE,3 SALISBURY ROAD, TSIM SHA TSUI, HONGKONG 999077, HK
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
HONG KONG ETECH GROUPS LIMITED (Owner Number: 10092912)
Owner / Operator Contact Address
ROOM 747,7/F,STAR HOUSE,3 SALISBURY ROAD, TSIM SHA TSUI, HONGKONG, HK-NOTA 999077, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Transcutaneous Electrical Nerve Stimulator (9029SCM) Humidifier Red Light Sound Machine, Model: MA1189, Red Light Alarm Clock Speaker, Model: MA1156 Smart Cupping 30357, 30590

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2025-03-05
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2025-03-05
KFZ Humidifier, Non-Direct Patient Interface (Home-Use) Anesthesiology Class 1 868.5460 2025-06-30
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2025-12-23
KNM Device, Pressure Applying Physical Medicine Class 1 890.5765 2025-08-04

Official Correspondent

No official correspondent registered.

US Agent Details

Jessie Yao Business: MEDRIGHT TECH INC Email: info@medright-tech.com Phone: (718) 2169957

Related Public Records

Same Entity

HONG KONG ETECH GROUPS 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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022929665. Last updated year: 2026. Please use registration number 3022929665 when referencing this establishment in official correspondence.
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