Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011949007

FEI Number

3011949007

Entity Name

KAI PORT OPTICAL MFG CO., LTD.

City/State/Country

Tainan, TW

Establishment Address

2F., No.168-1, Zhonglun, Anding Dist, Tainan 74554, TW

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Kai Port Optical Mfg Co., Ltd. (Owner Number: 10050235)

Owner / Operator Contact Address

2F., No.168-1, Zhonglun, Anding Dist, Tainan, TW-TNN 74554, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Frame Magnifying Spectacle

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2015-10-23
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2015-10-23

Official Correspondent

Li-Ting Huang

US Agent Details

Weian Huang Business: JOYSUN USA LLC Email: weian@isosh.com Phone: (949) 4624543

Related Public Records

Same Entity

Kai Port Optical Mfg 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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011949007. Last updated year: 2026. Please use registration number 3011949007 when referencing this establishment in official correspondence.