Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009307635

FEI Number

3009307635

Entity Name

DENTALL Co., Ltd.

City/State/Country

Bucheon-si Gyeonggi, KR

Establishment Address

301-905, Bucheontechnopark, 345, Seokcheon-ro, Ojeong-gu, Bucheon-si Gyeonggi 14501, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DENTALL Co., Ltd. (Owner Number: 10037262)

Owner / Operator Contact Address

301-905 Bucheontechnopark, 345, Seokcheon-ro, Ojeong-gu, Bucheon-si, KR-41 14501, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K170529

PMA Number

N/A

All Registered Proprietary Names

B&Lite S

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EBZ	Activator, Ultraviolet, For Polymerization	Dental	Class 2	872.6070	2017-08-12

Official Correspondent

Lee Jong Hyuk

US Agent Details

Jung Ryun Ahn Business: KMC USA, Inc Email: kmc.usa@kmcerti.com Phone: (646) 3576058

Related Public Records

Same Entity

DENTALL Co., Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K243921	Foshan Coxo Medical Instrument Co., Ltd.	LED Curing Lights (DB686 HALO)	2025-04-11
K033201	Apoza Enterprise Co., Ltd.	LA500 BLUE LIGHT	2003-12-02

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3030126955	ONVET MEDICAL CANADA INC	TORONTO Ontario, CA
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009307635. Last updated year: 2026. Please use registration number 3009307635 when referencing this establishment in official correspondence.