FULL SUN, INC.

FDA Device Registration & Listing · Cianjhen District., Kaohsiung City, TW · Registration 3006356447

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
3006356447
FEI Number
3006356447
Entity Name
FULL SUN, INC.
City/State/Country
Cianjhen District., Kaohsiung City, TW
Establishment Address
10F.-18, No. 12, Fusing 4th Rd.,, Cianjhen District., Kaohsiung City 80661, TW
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
FULL SUN, INC. (Owner Number: 9103082)
Owner / Operator Contact Address
10F.-18, No. 12, Fusing 4th Rd.,, --, Cianjhen District, Kaohsiung, TW-NOTA 80661, TW
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
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2007-06-18
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2007-06-18
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2020-04-21
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2007-06-18

Official Correspondent

No official correspondent registered.

US Agent Details

Thomas Pang Business: kapo optik Email: kapo_optik@yahoo.com Phone: (626) 2266699

Related Public Records

Same Entity

FULL SUN, INC.
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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006356447. Last updated year: 2026. Please use registration number 3006356447 when referencing this establishment in official correspondence.
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