Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009608177

FEI Number

3009608177

Entity Name

RMEDICA Co., Ltd.

City/State/Country

Geumcheon-Gu Seoul, KR

Establishment Address

2-Dong 709-Ho (Gasan-Dong, IT Castle), 98, Gasan digital 2-ro, Geumcheon-Gu Seoul 08506, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Rmedica co., Ltd (Owner Number: 10040716)

Owner / Operator Contact Address

2-Dong 709-Ho (Gasan-Dong, IT Castle), 98, Gasan digital 2-ro, Geumcheon-gu, KR-11 08506, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

BK230818

PMA Number

N/A

All Registered Proprietary Names

Platelet and Plasma Separator for Bone Graft Handling, Dr.PRP-I Platelet and Plasma Separator for Bone Graft Handling, Dr.PRP Platelet and Plasma Separator for Bone Graft Handling, GC Dr.PRP

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ORG	Platelet And Plasma Separator For Bone Graft Handling	Hematology	Class 2	864.9245	2023-06-27

Official Correspondent

Seong-Ryul Cho

US Agent Details

Joyce Kwon Business: Provision Consulting Group, Inc. Email: ask@provisionfda.com Phone: (909) 4933276

Related Public Records

Same Entity

Rmedica 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 3009608177. Last updated year: 2026. Please use registration number 3009608177 when referencing this establishment in official correspondence.