Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017180717

FEI Number

3017180717

Entity Name

WENZHOU QIAONEI GLASSES CO., LTD

City/State/Country

Wenzhou Zhejiang, CN

Establishment Address

5F-006A Floor, Haichuang Mingdi Bulding 1, NO.545 Jinhai Third Road, Wenzhou Economic Technological Development Zone, Wenzhou Zhejiang 325000, CN

Establishment Type(s)

Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

WENZHOU QIAONEI GLASSES CO., LTD (Owner Number: 10075157)

Owner / Operator Contact Address

5F-006A Floor, Haichuang Mingdi Bulding 1, NO.545 Jinhai Third Road, Wenzhou Economic Technological Development Zone, Wenzhou, CN-ZJ 325000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Spectacle, magnifying Frame, spectacle

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2020-06-08
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2020-06-08

Official Correspondent

Juhua Wu

US Agent Details

Fanny Zhao Business: J & F Technology Service Email: info@jf-yiliao.com Phone: (909) 5100201

Related Public Records

Same Entity

WENZHOU QIAONEI 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 3017180717. Last updated year: 2026. Please use registration number 3017180717 when referencing this establishment in official correspondence.