D.I. WARE COMPANY

FDA Device Registration & Listing · HONG KONG, HK · Registration 3005312815

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
3005312815
FEI Number
3005312815
Entity Name
D.I. WARE COMPANY
City/State/Country
HONG KONG, HK
Establishment Address
Flat E 9/F Tower 1 Sausalito, Yuk Tai Street, MA ON SHAN SHATIN, HONG KONG --, HK
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
D.I. WARE COMPANY (Owner Number: 9076559)
Owner / Operator Contact Address
RM 2, 23F, KAM DAT HSE, KAM YING COURT, MA ON SHAN SHATIN, HONG KONG, HK-NOTA --, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2005-08-17
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2014-08-06

Official Correspondent

Wing Ki Chui

US Agent Details

Lisa Wright Business: Vision Council Email: fda@thevisioncouncil.org Phone: (703) 5484560

Related Public Records

Same Entity

D.I. WARE COMPANY
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
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
K853921 Winsburn Company , Ltd. ALL KINDS OF SUNGLASSES 1985-10-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005312815. Last updated year: 2026. Please use registration number 3005312815 when referencing this establishment in official correspondence.
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