WENZHOU SUMMER INTERNATIONAL LIMITED

FDA Device Registration & Listing · Wenzhou Zhejiang, CN · Registration 3010329856

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
3010329856
FEI Number
3010329856
Entity Name
WENZHOU SUMMER INTERNATIONAL LIMITED
City/State/Country
Wenzhou Zhejiang, CN
Establishment Address
Room 201, No.24, Liming Industrial,, Wenzhou Zhejiang 325000, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
WENZHOU SUMMER INTERNATIONAL LIMITED (Owner Number: 10044703)
Owner / Operator Contact Address
Room 201, No.24, Liming Industrial,, Wenzhou, CN-ZJ 325000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Optical Frame Spectacle Frame Goggles Safety glasses Sunglasses Blue light blocked glasses SG24101 Spectacle Lens Reading glasses, presbyopic glasses

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2013-07-17
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2020-03-31
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2013-07-17
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2013-07-17

Official Correspondent

No official correspondent registered.

US Agent Details

Dike Yu Email: Fdaamerican@gmail.com Phone: (347) 9186666

Related Public Records

Same Entity

WENZHOU SUMMER INTERNATIONAL 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
K940726 Jay-Y Enterprises Co., Inc. NONE-GENERIC 1994-04-11
K934837 Simon Marketing, Inc. SUNGLASSES 1993-12-08
K852902 Yours Enterprise Co., Ltd. METALLIC SUNGLASSES 1985-08-12
K970895 Custom Optical Frames, Inc. CUSTOM OPTICAL SUNGLASS FRAMES 1997-05-06

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3013507321 DEM FACTORY S.R.L. Limana Belluno, IT
3015243992 L.G.R SRL Roma, IT
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010329856. Last updated year: 2026. Please use registration number 3010329856 when referencing this establishment in official correspondence.
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