Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010773581

FEI Number

3010773581

Entity Name

CENTRON CORPORATION

City/State/Country

Anyang-si Gyeonggi, KR

Establishment Address

44 Beolmal-ro, Dongan-gu, Anyang-si Gyeonggi 14059, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Centron Corporation (Owner Number: 10045761)

Owner / Operator Contact Address

44 Beolmal-ro, Dongan-gu, Anyang-si, KR-41 14059, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TUBE SEALER SE9 TUBE SEALER SE540 TUBE SEALER SE160 TUBE SEALER SE530 TUBE SEALER SE640 TUBE SEALER SE170 TUBE SEALER SE470RS TUBE SEALER SE330 TUBE SEALER SE340 TUBE SEALER SE7

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KSD	Device, Heat-Sealing	Hematology	Class 1	864.9750	2013-12-24

Official Correspondent

Jae Soon Kim

US Agent Details

Ethan Kim Business: CENTROVEST Email: jun@centrons.com Phone: (310) 3510951

Related Public Records

Same Entity

Centron Corporation

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 3010773581. Last updated year: 2026. Please use registration number 3010773581 when referencing this establishment in official correspondence.