Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005720077

FEI Number

3005720077

Entity Name

KYK CO.,LTD

City/State/Country

Seongnam-si Gyeonggi, KR

Establishment Address

(406,407) 555, Dunchon-daero, Jungwon-gu, Seongnam-si Gyeonggi 13215, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

KYK Co.,Ltd (Owner Number: 9086920)

Owner / Operator Contact Address

(406,407) 555, Dunchon-daero, Jungwon-gu, Seongnam-si, KR-41 13215, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

HYM3+ HIGEN1+ HYDROGEN TOX1 HIGEN2+ HIGEN3 HIGEN4+ GENERATION II RE3 KYK777 ML Ionizer-A3F HIGEN5+

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	2006-05-08

Official Correspondent

No official correspondent registered.

US Agent Details

Grace Kim Business: JS INTERNATIONAL HOLDING Email: ahn3060@naver.com Phone: (310) 5983012

Related Public Records

Same Entity

KYK 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 3005720077. Last updated year: 2026. Please use registration number 3005720077 when referencing this establishment in official correspondence.