Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012438919

FEI Number

3012438919

Entity Name

JBP KOREA CO.,LTD.

City/State/Country

Gangnam-gu Seoul, KR

Establishment Address

6F, 619, Gaepo-ro, Gangnam-gu Seoul 06336, KR

Establishment Type(s)

Foreign Private Label Distributor

Owner / Operator

JBP Korea Co.,Ltd. (Owner Number: 10055559)

Owner / Operator Contact Address

6F, 619, Gaepo-ro, Gangnam-gu, KR-11 06336, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

JBP V Line JBP V Line JBP V Line JBP Nano Cannula JBP Nanoneedle, JBP Nanoneedle Premier

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	2020-07-30
NEW	Suture, Surgical, Absorbable, Polydioxanone	General, Plastic Surgery	Class 2	878.4840	2026-04-20
NEW	Suture, Surgical, Absorbable, Polydioxanone	General, Plastic Surgery	Class 2	878.4840	2026-04-20
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2017-08-11

Official Correspondent

Hongseok Lim

US Agent Details

Bruce Handloff Business: JBP USA LLC Email: bhandloff@msn.com Phone: (831) 4191088

Related Public Records

Same Entity

JBP Korea 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
K812404	Nu Tech Medical Systems	BUTTERFLY NEEDLE ASSEMBLY	1981-09-09

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2022	Bard Peripheral Vascular Inc	2	REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012438919. Last updated year: 2026. Please use registration number 3012438919 when referencing this establishment in official correspondence.