Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023388535

FEI Number

3023388535

Entity Name

ILLUCO CO, LTD

City/State/Country

Gumpo-si Gyeonggi, KR

Establishment Address

SK Ventium Building 102, #304, 166 Gosan-ro, Gumpo-si Gyeonggi 15850, KR

Establishment Type(s)

Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Illuco Co, LTD (Owner Number: 10088918)

Owner / Operator Contact Address

SK Ventium Building 102, #304, 166 Gosan-ro, Gumpo-si, KR-41 15850, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

IDM-1C14-B IDM-1C14-DB IDS-1000 Plus IDS-1100C IDS-1000 ILHAC0002 (IHL-2000) IDS-9100 IDS-1100 IDS-3100 ILHAC0001 (IHL-1000) ITL-1055P IAL-1040A ITL-1025G IDS-1000 Plus ITL-1045P IAL-1030A IFL-1033G ITL-1033G ITL-1040P ITL-1035G ITL-1065P

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EAX	Mirror, Mouth	Dental	Class 1	872.4565	2025-01-26
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2023-10-20
FSP	Loupe, Diagnostic/Surgical	General, Plastic Surgery	Class 1	878.4800	2024-03-03

Official Correspondent

ILPYO HONG

US Agent Details

Justin Lee Business: TA Global Laboratories LLC Email: kayrico20000@gmail.com Phone: (213) 5005333

Related Public Records

Same Entity

Illuco Co, LTD

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023388535. Last updated year: 2026. Please use registration number 3023388535 when referencing this establishment in official correspondence.