Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007740684

FEI Number

3007740684

Entity Name

Suzhou Zhenwu Medical Co., Ltd.

City/State/Country

Suzhou Jiangsu, CN

Establishment Address

No.248, Chijiawan Road, Beishe Town, Fenhu Development Area, Wujiang District, Suzhou Jiangsu 215214, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Suzhou Zhenwu Medical Co., Ltd. (Owner Number: 10029917)

Owner / Operator Contact Address

No.248, Chijiawan Road, Beishe Town, Fenhu Development Area, Wujiang District, Suzhou, CN-JS 215214, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pull Blood Lancets 28G~36G Safety Lancets:Pressure Activated Safety Lancet(PA) 18G~36G Flat blood lancets 28G~36G Auto Lancets:Pressure Activated Safety Lancet(PA) 18G~36G Auto Lancets:Button Activated Safety Lancet(BA) 18G~36G Lancet Device with Ejector Safety Lancets:Button Activated Safety Lancet(BA) 18G~36G Splinter probe 18G~36G Twist Blood Lancets 18G~36G Lancing Devices With Blood Lancets omnis Lancing Devices S L Stainless Steel Blood Lancets S L M Nurse Rosie SensiLance Lancets with Pull Tops Blood Lancet

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2023-02-14
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2009-07-15

Official Correspondent

No official correspondent registered.

US Agent Details

LI QIAN Business: Carelife USA Inc. Email: li@carelifeusa.com Phone: (770) 9356499

Related Public Records

Same Entity

Suzhou Zhenwu Medical 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
K130132	Medipurpose Pte. , Ltd.	BABYLANCE HEEL INCISION DEVICE	2013-02-11

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0044-2008	Becton Dickinson & Company	2	Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

Similar Registrations

Registration Number	Establishment Name	Location
3004525100	SOYAGREENTEC CO.,LTD	Hwaseong-si Gyeonggi, KR
3004468256	SUZHOU KYUAN MEDICAL APPARATUS CO., LTD.	Suzhou City Jiangsu, CN
3010515547	PROMISEMED HANGZHOU MEDITECH CO.,LTD.	Hangzhou Zhejiang, CN
3012172036	TASSO INC	Seattle, WA, US
3012494290	SANICURE BV	SCHIPHOL Noord-Holland, NL

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007740684. Last updated year: 2026. Please use registration number 3007740684 when referencing this establishment in official correspondence.