Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020138744

FEI Number

3020138744

Entity Name

W.L.MED CO., LTD.

City/State/Country

Anseong-si Gyeonggi, KR

Establishment Address

246, Geumgwangosan-ro, Geumgwang-myeon, Anseong-si Gyeonggi 17535, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

W.L.Med Co., Ltd. (Owner Number: 10082898)

Owner / Operator Contact Address

246, Geumgwangosan-ro, Geumgwang-myeon, Anseong-si, KR-41 17535, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K210748

PMA Number

N/A

All Registered Proprietary Names

Well-life Pen Needles Well-life Safety Pen Needles

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2022-06-07

Official Correspondent

Young Chul Bang

US Agent Details

Peter Chung Email: peterchung210@gmail.com Phone: (412) 5128802

Related Public Records

Same Entity

W.L.Med 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 3020138744. Last updated year: 2026. Please use registration number 3020138744 when referencing this establishment in official correspondence.