Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008423561

FEI Number

3008423561

Entity Name

LIFETECH SCIENTIFIC (SHENZHEN) CO,.LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

8F, LifeTech Scientific Building, No.22, Keji 12th Road South, High-tech Industrial Park, Yuehai Subdistrict, Nanshan District, Shenzhen Guangdong 518063, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Lifetech Scientific (Shenzhen) Co,.Ltd (Owner Number: 10036342)

Owner / Operator Contact Address

8F, LifeTech Scientific Building, No.22, Keji 12th Road South, High-tech Industrial Park, Yuehai Subdistrict, Nanshan District, Shenzhen 518063, P. R. China., Shenzhen, CN-GD 518063, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K102484

PMA Number

N/A

All Registered Proprietary Names

LawMax Dilator FuStar SeQure

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DRE	Dilator, Vessel, For Percutaneous Catheterization	Cardiovascular	Class 2	870.1310	2013-11-27
DQY	Catheter, Percutaneous	Cardiovascular	Class 2	870.1250	2011-05-03
MMX	Device, Percutaneous Retrieval	Cardiovascular	Class 2	870.5150	2011-05-03

Official Correspondent

Zhang Yanhong

US Agent Details

Thomas Tang Email: usagent@cefda.com Phone: (631) 7511103

Related Public Records

Same Entity

Lifetech Scientific (Shenzhen) 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
K043580	Chestnut Medical Technologies, Inc.	ALLIGATOR RETRIEVAL DEVICE (ARD)	2005-03-24
K982883	Medtronics Interventional Vascular	MEDTRONIC 7F AND 8F ZUMA GUIDING CATHETER	1998-09-04
K132420	Reflow Medical	WINGMAN EXTENDABLE TIP SUPPORT CATHETER	2013-09-19
K082339	Endocross, Ltd.	ENABLER-P SUPPORT CATHETER	2008-11-20
K210009	CenterPoint Systems, LLC	Guiding Catheter	2021-11-24

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0001-2010	Penumbra Inc.	2	Penumbra Neuron Delivery Catheter 070, percutaneous catheter, catalog numbers PND6F0701058, PND6F070956, PND6F0701058M, and PND6F070956M; manufactured by Penumbra, Inc., Alameda, CA. Indicated for the introduction of interventional devices into the peripheral, coronary, and neuro vasculature.
Z-0003-2014	Cordis Corporation	2	Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular introduction of interventional and/or diagnostic devices into the coronary or peripheral vascular system.
Z-0009-2024	Boston Scientific Corporation	2	Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM, Catalog number H965100420, cardiac guide catheter
Z-0010-04	Bard Peripheral Vascular	2	Conquest Balloon Dilation Catheters Model/Catalog Number CQ 75124
Z-0010-2024	Boston Scientific Corporation	2	Guider Softip Guide Catheter 7F PRE-SHAPED 40 90CM, Catalog number H965100430, cardiac guide catheter

Similar Registrations

Registration Number	Establishment Name	Location
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3011642792	Merit Maquiladora Mexico, S. DE R.L. DE C.V.	Tijuana Baja California, MX
3006950086	Merit Medical Nederland BV	Maastricht Airport Limburg, NL
3015225571	Merit Medical Asia Company Limited	Tsim Sha Tsui, HK
3006082230	C.R. BARD, INC.	MADISON, GA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008423561. Last updated year: 2026. Please use registration number 3008423561 when referencing this establishment in official correspondence.