WENZHOU HALA TRADE CO.LTD

FDA Device Registration & Listing · Wenzhuo Zhejiang, CN · Registration 3012796531

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
3012796531
FEI Number
3012796531
Entity Name
WENZHOU HALA TRADE CO.LTD
City/State/Country
Wenzhuo Zhejiang, CN
Establishment Address
Room 507, Wenzhou Dadao 1780,Lucheng district, Wenzhuo Zhejiang 325000, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Wenzhou Hala Trade Co.Ltd (Owner Number: 10081338)
Owner / Operator Contact Address
Room 507, Wenzhou Dadao 1780,Lucheng district, Wenzhuo, 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 lens optical frame , KEA , GILA Set, lens, trial Spectacles, magnifying Shield, eye spare parts

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2021-04-06
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2021-04-06
HPC Set, Lens, Trial, Ophthalmic Ophthalmic Class 1 886.1405 2021-04-06
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2021-04-06
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2021-04-06
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2021-04-06

Official Correspondent

Jessie Huang

US Agent Details

Wilson Li Email: qagujdsvvt@outlook.com Phone: (719) 2013315

Related Public Records

Same Entity

Wenzhou Hala Trade 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
K900478 Woodlyn, Inc. WOODLYN FULL APERTURE TRIAL LENS SET 1990-02-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012796531. Last updated year: 2026. Please use registration number 3012796531 when referencing this establishment in official correspondence.
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