Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015969621

FEI Number

3015969621

Entity Name

TAIZHOU DUOYING GLASSES CO.,LTD.

City/State/Country

Taizhou Zhejiang, CN

Establishment Address

South Side of Donghai No.1 Avenue, South Industrial Zone, Duqiao Town, Linhai, Taizhou Zhejiang 317016, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Taizhou Duoying Glasses Co.,Ltd. (Owner Number: 10061343)

Owner / Operator Contact Address

South Side of Donghai No.1 Avenue, South Industrial Zone, Duqiao Town, Linhai, Taizhou, CN-ZJ 317016, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Spectacle, magnifying

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2019-10-10

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

Taizhou Duoying Glasses Co.,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 3015969621. Last updated year: 2026. Please use registration number 3015969621 when referencing this establishment in official correspondence.