Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013589761

FEI Number

3013589761

Entity Name

YURIM MEDICAL CO.,LTD

City/State/Country

Cheongju-si Chungbuk, KR

Establishment Address

43, Jeongjung 3-gil, Osong-eup, Heungdeok-gu, Cheongju-si Chungbuk 28164, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

YURIM MEDICAL CO.,LTD (Owner Number: 10060750)

Owner / Operator Contact Address

43, Jeongjung 3-gil, Osong-eup, Heungdeok-gu, Cheongju-si, KR-43 28164, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PDO Max Suture with Dual Needle

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NEW	Suture, Surgical, Absorbable, Polydioxanone	General, Plastic Surgery	Class 2	878.4840	2025-07-30
GEA	Cannula, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2020-01-08

Official Correspondent

Hae June Yahng

US Agent Details

Robert Packard Business: Medical Device Academy Incorporated Email: rob@fdaestar.com Phone: (802) 2581881

Related Public Records

Same Entity

YURIM MEDICAL 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
K863293	Lifestream Int'L, Inc.	DISPOSABLE SUCTION CANNULA NO. 902008-000	1986-09-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013589761. Last updated year: 2026. Please use registration number 3013589761 when referencing this establishment in official correspondence.