TIANJIN RILIFINE MEDICAL DEVICE CO.,LTD

FDA Device Registration & Listing · Tianjin, CN · Registration 3021314645

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
3021314645
FEI Number
3021314645
Entity Name
TIANJIN RILIFINE MEDICAL DEVICE CO.,LTD
City/State/Country
Tianjin, CN
Establishment Address
No 32, Jingguan Road, Yixingbu, Beichen District, Tianjin 300402, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Tianjin Rilifine Medical Device Co.,Ltd (Owner Number: 10083487)
Owner / Operator Contact Address
No 32, Jingguan Road, Yixingbu, Beichen District, Tianjin, CN-NOTA 300402, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Lancing device, Disposable Sterile Lancet: Twist Lancet; Model I; Specification: 17G, 18G, 19G, 20G, 21G, 22G, 23G, 24G, 25G, 26G, 27G, 28G, 29G, 30G, 31G, 32G, 33G, 34G Specification: 17G, 18G, 19G, 20G, 21G, 22G, 23G, 24G, 25G, 26G, 27G, 28G, 29G, 30G, 31G, 32G, 33G, 34G Disposable Sterile Lancet: Safety Lancet; Model II; Lancet,Blood lancets,Lancing device,Lancet device,Safety lancet,Twist lancet

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QRK Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature General, Plastic Surgery Class 2 878.4850 2022-12-01
QRL Multiple Use Blood Lancet For Single Patient Use Only General, Plastic Surgery Class 2 878.4850 2022-12-01
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature General, Plastic Surgery Class 2 878.4850 2022-12-01
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature General, Plastic Surgery Class 2 878.4850 2021-11-23

Official Correspondent

Henry Jiang

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Tianjin Rilifine Medical Device 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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021314645. Last updated year: 2026. Please use registration number 3021314645 when referencing this establishment in official correspondence.
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