Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010462274

FEI Number

3010462274

Entity Name

FEELTECH CO.,LTD.

City/State/Country

Gunsan-si Jeonbuk, KR

Establishment Address

4 Floor, Standard Factory 5-dong, part of 1 Floor, Standard Factory 1-dong, part of 3, 4 Floor, Standard Factory 2-dong,15, Jayumuyeok 2-gil, Gunsan-si Jeonbuk 54001, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Feeltech Co.,Ltd. (Owner Number: 10050336)

Owner / Operator Contact Address

Standard Factory 1-dong(1F), 2-dong(3F, 4F), 5-dong(4F),, 15, Jayumuyeok 2-gil, Gunsan-si, KR-45 54001, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

JBP V Line Suture, Surgical, Absorbable, Polydioxanone, - Miracu; ELASTY; V Soft Line Syringe, Piston- Feelject Suture, Surgical, Absorbable, Polydioxanone, - Miracu; ELASTY; V Soft Line JBP V Line FEELject LDV(Low dead volume) Syringe IdryNeedle (DN150, DN161)

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	2026-01-08
FMF	Syringe, Piston	General Hospital	Class 2	880.5860	2021-05-25
NEW	Suture, Surgical, Absorbable, Polydioxanone	General, Plastic Surgery	Class 2	878.4840	2026-01-08
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2024-06-06
QNQ	Low Dead Space Piston Syringe	General Hospital	Class 2	880.5860	2024-06-06
MQX	Needle, Acupuncture, Single Use	General Hospital	Class 2	880.5580	2020-01-11

Official Correspondent

Geun Sik Kim

US Agent Details

Kelly Kim Business: Kelly Medical Consulting Email: kmedcon@yahoo.com Phone: (949) 2937124

Related Public Records

Same Entity

Feeltech 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
K880350	Honway International Co.	YUE/FA DISPOSABLE SYRINGE	1988-02-16
K003571	Terumo Medical Corp.	SERONO FOR USE WITH GONAL-F 1200IU MULTI-DOSE ONLY AT 600IU/ML SYRINGE	2001-02-12
K812404	Nu Tech Medical Systems	BUTTERFLY NEEDLE ASSEMBLY	1981-09-09

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0003-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 30G X 5/16'' syringes
Z-0004-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1 cc X 29G X 1/2 '' insulin syringes
Z-0005-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 29G X 1/2 '' insulin syringes
Z-0005-2024	Fresenius Medical Care Holdings, Inc.	2	10ML SYRINGE LUER LOCK W/OUT NEEDLE, Part Number 15-R010-0, 100 per box, 12 boxes to a case
Z-0006-2024	Fresenius Medical Care Holdings, Inc.	2	10ML SYRINGE LUER LOCK W/NEEDLE, Part Number 15-10ML-0, 100 per box, 12 boxes per case

Similar Registrations

Registration Number	Establishment Name	Location
3017936846	BELLA TECH GLOBAL INC	Brea, CA, US
3017102971	ETHICON, INC.	Raritan, NJ, US
3006638824	ETHICON, INC.	CIUDAD JUAREZ Chihuahua, MX
3013557562	CBR ENTERPRISE LIMITED	Hong Kong, HK
1221601	Teleflex Medical LLC	MANSFIELD, MA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010462274. Last updated year: 2026. Please use registration number 3010462274 when referencing this establishment in official correspondence.