Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015168743

FEI Number

3015168743

Entity Name

D&D ELECTRONICS CO., LTD.

City/State/Country

Anyang-si Gyeonggi, KR

Establishment Address

#207, Megavalley, 268, Hagui-ro, Dongan-gu, Anyang-si Gyeonggi 14056, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

D&D Electronics Co., Ltd. (Owner Number: 10059520)

Owner / Operator Contact Address

#207, Megavalley, 268, Hagui-ro, Dongan-gu, Anyang-si, KR-41 14056, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DES-P800 DES-P350 DES-WA50 DES-16000PRO DES-10K DES-S50 DES-4000 DES-16000 DES-WS850 DES-4000PRO DES-10K-S DES-P350S Electrolyzed water by NaOClean Generator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JRS	Purifier, Water (Absorption, Deionization, Membrane Filter, Reverse Osmosis)	Clinical Chemistry	Class 1	862.2050	2021-10-31
LRJ	Disinfectant, Medical Devices	General Hospital	Class 1	880.6890	2019-01-30

Official Correspondent

No official correspondent registered.

US Agent Details

Jongoh CHOO Business: SMGUSA LLC Email: ce@smgusa.org Phone: (307) 6502347

Related Public Records

Same Entity

D&D Electronics 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 3015168743. Last updated year: 2026. Please use registration number 3015168743 when referencing this establishment in official correspondence.