GOLDEN AIM INTERNATIONAL LTD

FDA Device Registration & Listing · Shenzhen City,, GUANGDONG, CHINA, HK · Registration 3009523076

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
3009523076
FEI Number
3009523076
Entity Name
GOLDEN AIM INTERNATIONAL LTD
City/State/Country
Shenzhen City,, GUANGDONG, CHINA, HK
Establishment Address
Room 2012-2013, 20/F, Tower A, Youcheng Business Building, No. 567 Minzhi Road, Shenzhen City,, GUANGDONG, CHINA 518131, HK
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Golden Aim International LTD (Owner Number: 10039389)
Owner / Operator Contact Address
Unit A, 14/F Hua Chiao Commercial Centre, 678 Nathan Road, Mong Kok, HK-NOTA 0000000, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Re-chargeable hot water bottle Tonific Bio Feedbac Massager Knee Brace

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2013-12-02
KCX Epilator, High Frequency, Tweezer-Type General, Plastic Surgery Class 1 878.5360 2012-11-28
ITW Joint, Ankle, External Brace Physical Medicine Class 1 890.3475 2014-02-27
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2012-06-19
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2013-07-10

Official Correspondent

Mimi Ying

US Agent Details

Bob Smith Email: info@globaltvconcepts.com Phone: (561) 2899813

Related Public Records

Same Entity

Golden Aim International LTD
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009523076. Last updated year: 2026. Please use registration number 3009523076 when referencing this establishment in official correspondence.
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