TAIZHOU YIZHAN OPTICAL GLASSES CO., LTD

FDA Device Registration & Listing · Taizhou City Zhejiang, CN · Registration 3021343301

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
3021343301
FEI Number
3021343301
Entity Name
TAIZHOU YIZHAN OPTICAL GLASSES CO., LTD
City/State/Country
Taizhou City Zhejiang, CN
Establishment Address
No 101 Unit Building 5, Glasses Pioneer Park, Donghai First Avenue, Duqiao District, Linhai City, Taizhou City Zhejiang 317016, CN
Establishment Type(s)
Manufacture Medical Device,Foreign Private Label Distributor
Owner / Operator
Taizhou Yizhan Optical Glasses Co., Ltd (Owner Number: 10083592)
Owner / Operator Contact Address
No 101 Unit Building 5, Glasses Pioneer Park, Donghai First Avenue, Duqiao District, Linhai City, Taizhou City, CN-ZJ 317016, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
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
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2021-12-03
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2021-12-03

Official Correspondent

Ming Jun Lo

US Agent Details

WAYNE CHEN Business: GOT SHADES INTERNATIONAL Email: wayne@gotshades.com Phone: (909) 7187866

Related Public Records

Same Entity

Taizhou Yizhan Optical Glasses Co., Ltd
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 3021343301. Last updated year: 2026. Please use registration number 3021343301 when referencing this establishment in official correspondence.
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