KNK

FDA Device Registration & Listing · Yeondong-myeon Sejong, KR · Registration 3018783126

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
3018783126
FEI Number
3018783126
Entity Name
KNK
City/State/Country
Yeondong-myeon Sejong, KR
Establishment Address
119, Myeonghaksandan-ro, Yeondong-myeon Sejong 30068, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KNK (Owner Number: 10081488)
Owner / Operator Contact Address
119, Myeonghaksandan-ro, Yeondong-myeon, KR-50 30068, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Glister Multi-Action Power Toothbrush Glister Multi-Action Power Toothbrush Refill

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JEQ Toothbrush, Powered Dental Class 1 872.6865 2024-04-04

Official Correspondent

No official correspondent registered.

US Agent Details

Grace Kim Business: J.S. CHEM INTERNATIONAL CO. Email: gracejschem@hotmail.com Phone: (310) 5983012

Related Public Records

Same Entity

KNK
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 3018783126. Last updated year: 2026. Please use registration number 3018783126 when referencing this establishment in official correspondence.
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