Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031600752

FEI Number

3031600752

Entity Name

ACTCELLBIO CO., LTD.

City/State/Country

Gwangmyeong-si Gyeonggi, KR

Establishment Address

B-614, 190, Soha-ro, Gwangmyeong-si Gyeonggi 14322, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ACTcellBIO CO., LTD. (Owner Number: 10091081)

Owner / Operator Contact Address

B-614, 190, Soha-ro, Gwangmyeong-si, KR-41 14322, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ACT PRP DB30 ACT PRP ACT BMS 30 ACT PRF

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KET	Filters, Cell Collection, Tissue Processing	Pathology	Class 1	864.3010	2024-06-26

Official Correspondent

Ray Jeon

US Agent Details

Peter Chung Business: Plus Global Email: peterchung210@gmail.com Phone: (412) 6873976

Related Public Records

Same Entity

ACTcellBIO 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 3031600752. Last updated year: 2026. Please use registration number 3031600752 when referencing this establishment in official correspondence.