Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003723176

FEI Number

3008801456

Entity Name

SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO. LTD.

City/State/Country

JINAN Shandong, CN

Establishment Address

No.1 Shuangshan Sanjian Road,, Zhangqiu, JINAN Shandong 250200, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO. LTD. (Owner Number: 9050813)

Owner / Operator Contact Address

No.1 Shuangshan Sanjian Road,, Zhangqiu, Jinan, CN-SD 250200, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K222472

PMA Number

N/A

All Registered Proprietary Names

Safety Lancet NPA Safety Lancet PA Lianfa Safety Lancet Safety Lancet TPA Safety Lancet PAII Safety Lancet APA ONE-CARE Safety Lancets Sterile Lancet for Single Use Twist Lancet Lancing Device Lancing System Embrace Lancing Device With Ejector Embrace Sterile 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	2022-12-03
QRL	Multiple Use Blood Lancet For Single Patient Use Only	General, Plastic Surgery	Class 2	878.4850	2022-12-03
QRK	Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2022-12-03

Official Correspondent

David Zhou

US Agent Details

Dennis Xu Business: Performance Internatinoal Inc. Email: Ybx99@yahoo.com Phone: (919) 8590478

Related Public Records

Same Entity

SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS 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 3003723176. Last updated year: 2026. Please use registration number 3003723176 when referencing this establishment in official correspondence.