Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009645513

FEI Number

3009645513

Entity Name

MAXI EYE

City/State/Country

Daegu Gyeongbuk, KR

Establishment Address

76, Nowon-ro, Buk- gu,, Daegu Gyeongbuk 41557, KR

Establishment Type(s)

Foreign Private Label Distributor,Manufacture Medical Device

Owner / Operator

MAXI EYE (Owner Number: 10041700)

Owner / Operator Contact Address

76 Nowon-ro, Buk-gu,, Daegu, KR-47 41557, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MAXI EYE EYEGLASS FRAME

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2012-08-21

Official Correspondent

SUK IK SON

US Agent Details

Won Woo Suh Business: HSchem America Email: mjk11@hotmail.com Phone: (213) 5597719

Related Public Records

Same Entity

MAXI EYE

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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3009554831	ROGER EYE DESIGN	Etten-Leur Noord-Brabant, NL
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009645513. Last updated year: 2026. Please use registration number 3009645513 when referencing this establishment in official correspondence.