JEIL TECH CO.,LTD

FDA Device Registration & Listing · Sejong-si Daegu, KR · Registration 3007774504

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007774504
FEI Number
3007774504
Entity Name
JEIL TECH CO.,LTD
City/State/Country
Sejong-si Daegu, KR
Establishment Address
190, Maesil-ro, Sojeong-myeon,, Sejong-si Daegu 339871, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
JEIL TECH Co.,Ltd (Owner Number: 10042692)
Owner / Operator Contact Address
190, Maesil-ro, Sojeong-myeon,, Sejong-si, KR-NOTA 339871, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Sterile Single-use LDV Syringe CHOICARE Sterile Single-use LDV Syringe

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QNQ Low Dead Space Piston Syringe General Hospital Class 2 880.5860 2023-04-03
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2023-04-03

Official Correspondent

Chun Gi Lee

US Agent Details

Priscilla Chung Business: LK Consulting Group USA, Inc. Email: juhee.c@lkconsultinggroup.com Phone: (714) 9225276

Related Public Records

Same Entity

JEIL TECH 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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3014312726 Sol-Millennium Medical, Inc. Chicago, IL, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007774504. Last updated year: 2026. Please use registration number 3007774504 when referencing this establishment in official correspondence.
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