Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014242973

FEI Number

3014242973

Entity Name

BESTSEA-TECH LIMITED

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

NO.1002, Building 4, Bangyan Green Valley Factory Building, No. 98, Zhihe Road, Dakang, Yuanshan Street, Longgang, Shenzhen Guangdong 518115, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

BESTSEA-TECH LIMITED (Owner Number: 10056908)

Owner / Operator Contact Address

NO.1002, Building 4, Bangyan Green Valley Factory Building, No. 98, Zhihe Road, Dakang, Yuanshan Street, Longgang, Shenzhen, CN-GD 518115, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Spectacle Frame

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2022-08-28

Official Correspondent

IVEN ZHONG

US Agent Details

Wei Huang Email: weihuang1979@gmail.com Phone: (713) 5053208

Related Public Records

Same Entity

BESTSEA-TECH 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
K910951	United Optical, Spa	OPTHLAMIC FRAMES	1991-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014242973. Last updated year: 2026. Please use registration number 3014242973 when referencing this establishment in official correspondence.