Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3039304811

FEI Number

3039304811

Entity Name

SOLEX HIGH-TECH INDUSTRIES (VIETNAM) COMPANY LIMITED

City/State/Country

Quang Yen Town Quang Ninh, VN

Establishment Address

Land Plot CN1.2A, Bac Tien Phong Industrial Zone, Quang Yen Town Quang Ninh 02220, VN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

SOLEX HIGH-TECH INDUSTRIES (VIETNAM) COMPANY LIMITED (Owner Number: 10093717)

Owner / Operator Contact Address

Land Plot CN1.2, Bac Tien Phong Industrial Zone, Lien Hoa Ward, Quang Ninh Province, /, VN-13 02220, VN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Light Based Over The Counter Wrinkle Reduction Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction - Titan Mini; Titan MultiPlatform; Silk'n Titan Allways Light Based Over The Counter Wrinkle Reduction - Titan Mini; Titan MultiPlatform; Silk'n Titan Allways

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OHS	Light Based Over The Counter Wrinkle Reduction	General, Plastic Surgery	Class 2	878.4810	2025-06-26
OHS	Light Based Over The Counter Wrinkle Reduction	General, Plastic Surgery	Class 2	878.4810	2025-06-26
PAY	Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction	General, Plastic Surgery	Class 2	878.4420	2025-06-26

Official Correspondent

Zhi Hui Wu

US Agent Details

Hui Hong Business: ABMED MEDICAL TECHNOLOGY INC Email: info@abmed.us Phone: (303) 8000162

Related Public Records

Same Entity

SOLEX HIGH-TECH INDUSTRIES (VIETNAM) COMPANY LIMITED

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 3039304811. Last updated year: 2026. Please use registration number 3039304811 when referencing this establishment in official correspondence.