ID KOREA CO., LTD.

FDA Device Registration & Listing · Dong-gu Gwangju, KR · Registration 3039359767

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
3039359767
FEI Number
3039359767
Entity Name
ID KOREA CO., LTD.
City/State/Country
Dong-gu Gwangju, KR
Establishment Address
405, 150, Donggyecheon-ro, Dong-gu Gwangju 61436, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ID KOREA CO., LTD. (Owner Number: 10093594)
Owner / Operator Contact Address
405, 150, Donggyecheon-ro, Dong-gu, KR-29 61436, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

ID Light Cure System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQC Mouthguard, Prescription Unknown Class U N/A 2025-06-10
KMY Positioner, Tooth, Preformed Dental Class 1 872.5525 2025-06-10
EBF Material, Tooth Shade, Resin Dental Class 2 872.3690 2025-06-10
EBD Coating, Filling Material, Resin Dental Class 2 872.3310 2025-06-10
EBI Resin, Denture, Relining, Repairing, Rebasing Dental Class 2 872.3760 2025-06-10

Official Correspondent

Youngbin Kim

US Agent Details

YONG O KIM Business: ID AMERICA LLC Email: tommey777@gmail.com Phone: (972) 9946817

Related Public Records

Same Entity

ID KOREA 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
K952662 Jeneric/Pentron, Inc. COMP=FLOW 1995-08-28
K171147 Bisco, Inc. REVEAL Bulk 2017-08-04
K770922 Espe GmbH (Us) DENTAL RESTORATIVE IN CAPSULES 1977-06-01
K153476 Kuraray Noritake Dental, Inc. KATANA AVENCIA Block 2016-08-23
K093019 Enamelite, LLC ENAMELITE ACRYSEAL SPRAY SEALANT 2009-12-22

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0028-2020 Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany 2
Grandio SO Heavy Flow Caps, Color A3 - Product Usage: Filling minimally invasive cavities of all classes - Filling small class I cavities and extended fissure sealing - Filling class II - V cavities including V-shaped defects and cervical caries - Blocking out undercuts - Lining or coating cavities - Repairing fillings and veneers - Luting translucent prosthetic pieces (e.g., full ceramic crowns, etc.).

Similar Registrations

Registration Number Establishment Name Location
3025434480 TMJ SERVICES LLC Franklin, TN, US
3030268763 OWL DENTAL San Leandro, CA, US
3008320092 Shandong Huge Dental Material Corporation Rizhao Shandong, CN
3005942449 Amann Girrbach North America, LP Charlotte, NC, US
2086043 PAC-DENT INC. Brea, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039359767. Last updated year: 2026. Please use registration number 3039359767 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.