VIETNAM AISHI OPTICS COMPANY LIMITED

FDA Device Registration & Listing · Lang Giang District Bac Ninh, VN · Registration 3038278924

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
3038278924
FEI Number
3038278924
Entity Name
VIETNAM AISHI OPTICS COMPANY LIMITED
City/State/Country
Lang Giang District Bac Ninh, VN
Establishment Address
A part of Lot CN03 (CN03.5), Tan Hung Industrial Park, Lang Giang District Bac Ninh 230000, VN
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
VIETNAM AISHI OPTICS COMPANY LIMITED (Owner Number: 10093323)
Owner / Operator Contact Address
A Part of Lot CN-03 (CN-03.5), Tan Hung Industrial Park, Lang Giang Commune, VN-56 230000, VN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Eyewear Spectacle Frame

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 2025-04-30
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2025-04-30
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2025-04-30

Official Correspondent

Honghai Chen

US Agent Details

Patrick Wong Email: patrick@aishioptics.com Phone: (917) 8824763

Related Public Records

Same Entity

VIETNAM AISHI OPTICS COMPANY 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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038278924. Last updated year: 2026. Please use registration number 3038278924 when referencing this establishment in official correspondence.
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