Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014397113

FEI Number

3014397113

Entity Name

MBD CO., LTD.

City/State/Country

Suwon-si Gyeonggi, KR

Establishment Address

B-8,9F, 145, Gwanggyo-ro, Yeongtong-gu, Suwon-si Gyeonggi 16229, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MBD Co., Ltd. (Owner Number: 10060767)

Owner / Operator Contact Address

B-8,9F, 145, Gwanggyo-ro, Yeongtong-gu, Suwon-si, KR-41 16229, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ASFA Shaker ASFA SPOTTER ASFA SCANNER ASFA Chopper

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JRQ	Shaker/Stirrer	Clinical Chemistry	Class 1	862.2050	2024-08-15
JTC	Device, Microtiter Diluting/Dispensing	Microbiology	Class 1	866.2500	2019-09-17
KHO	Fluorometer, For Clinical Use	Clinical Chemistry	Class 1	862.2560	2019-06-20
LEC	Grinder, Tissue	Pathology	Class 1	864.3010	2024-08-15

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

MBD 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 3014397113. Last updated year: 2026. Please use registration number 3014397113 when referencing this establishment in official correspondence.