Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3024844185

FEI Number

3024844185

Entity Name

DFIX

City/State/Country

GIMPO Gyeonggi, KR

Establishment Address

127 Gimpohangang 10-ro 133beon-gil, GIMPO Gyeonggi 10071, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DFIX (Owner Number: 10086273)

Owner / Operator Contact Address

127 Gimpohangang 10-ro 133beon-gil, GIMPO, KR-41 10071, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SDFIX DIALFIX PLUS DIALFIX

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMK	Device, Intravascular Catheter Securement	General Hospital	Class 1	880.5210	2022-10-27
MKY	System, Skin Closure	General, Plastic Surgery	Class 1	878.4320	2022-10-26

Official Correspondent

No official correspondent registered.

US Agent Details

David Hyun Jun Paek Email: dpaek.rennes@gmail.com Phone: (818) 9030660

Related Public Records

Same Entity

DFIX

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 3024844185. Last updated year: 2026. Please use registration number 3024844185 when referencing this establishment in official correspondence.