Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006973644

FEI Number

3006973644

Entity Name

DURICO C&T, INC.

City/State/Country

Sangju-si Gyeongbuk, KR

Establishment Address

33, Oedap 6-Gil, Sangju-si Gyeongbuk 37240, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Durico C&T, Inc. (Owner Number: 10025133)

Owner / Operator Contact Address

Oedap 6-Gil, 33, Sangju-Si, KR-47 37240, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Ulstar Durico

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LMD	System, Digital Image Communications, Radiological	Radiology	Class 1	892.2020	2008-03-17

Official Correspondent

Joo Wan Kim

US Agent Details

Eric Jibum Lee Email: sales@duricoimaging.com Phone: (714) 5217000

Related Public Records

Same Entity

Durico C&T, Inc.

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 3006973644. Last updated year: 2026. Please use registration number 3006973644 when referencing this establishment in official correspondence.