ZIBO QICHUANG MEDICAL PRODUCTS CO.,LTD.

FDA Device Registration & Listing · Zibo Shandong, CN · Registration 3015416207

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
3015416207
FEI Number
3015416207
Entity Name
ZIBO QICHUANG MEDICAL PRODUCTS CO.,LTD.
City/State/Country
Zibo Shandong, CN
Establishment Address
No.777 Changzheng Road new&hi-tech, Zibo Shandong 255000, CN
Establishment Type(s)
Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Zibo Qichuang Medical Products Co.,Ltd. (Owner Number: 10061488)
Owner / Operator Contact Address
No.777 Changzheng Road new&hi-tech, Zibo, CN-SD 255000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Face shield Mask plastic tray non woven wound dressing, Foam dressing Tourniquet IV start kit Urine bag catheter securement device suction tube Cap tongue depressor Medical kit Gauze, absorbent pad sponge brush medical tape, Band-aid, bandage plastic speculum swab stick Gown Forceps, medical pliers

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPY Shield, Protective, Personnel Radiology Class 1 892.6500 2020-03-28
LYU Accessory, Surgical Apparel General, Plastic Surgery Class 1 878.4040 2020-03-28
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2019-10-23
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2019-10-23
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2019-10-23
LRS I.V. Start Kit General Hospital Class 2 880.5200 2023-06-06
LRW Scissors, General, Surgical General, Plastic Surgery Class 1 878.4800 2019-10-23
CBH Device, Fixation, Tracheal Tube Anesthesiology Class 1 868.5770 2019-10-23
JOL Catheter And Tip, Suction General Hospital Class 2 880.6740 2019-10-23
FYF Cap, Surgical General, Plastic Surgery Class 1 878.4040 2019-10-23
FMA Depressor, Tongue, Non-Surgical General Hospital Class 1 880.6230 2019-10-23
KDD Kit, Surgical Instrument, Disposable General, Plastic Surgery Class 1 878.4800 2019-10-23
FRL Fiber, Medical, Absorbent General Hospital Class 1 880.5300 2019-10-23
GEC Brush, Scrub, Operating-Room General, Plastic Surgery Class 1 878.4800 2019-10-23
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2019-10-23
HIB Speculum, Vaginal, Nonmetal Obstetrics/Gynecology Class 2 884.4530 2019-10-23
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2019-10-23
FME Gown, Examination General Hospital Class 1 880.6265 2019-10-23
HTD Forceps General, Plastic Surgery Class 1 878.4800 2019-10-23

Official Correspondent

WENHAI Ma

US Agent Details

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

Related Public Records

Same Entity

Zibo Qichuang Medical 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
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04
K852723 The Huxley Instrument Corp. FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420 1985-07-15

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2016 Zimmer, Inc. 1
Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.
Z-0007-2013 Invuity, Inc. 2
BriteField illuminated Suction Device; Model numbers 8Fr, 10Fr and 12Fr, Kit (included 8Fr, 10Fr and 12Fr and a sterilization tray. The Invuity Brite Field Illuminated Suction Device is intended to aspirate from the surgical site and to provide illumination from a high intensity light source.

Similar Registrations

Registration Number Establishment Name Location
3000174892 CANADIAN SCIENTIFIC PRODUCTS LTD. DBA CSP MEDICAL London Ontario, CA
3029900933 LEMER PAX AMERICA Montreal Quebec, CA
3043535425 K-ONE MEDITECH SDN. BHD. Sekinchan Selangor, MY
3005257704 BEIJING KELIDA MEDICAL EQUIPMENT DEVELOPING CO., LTD Beijing City, CN
3016948452 QINHUANGDAO TAIZHI MEDICAL TECHNOLOGY CO., LTD Qinhuangdao Hebei, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015416207. Last updated year: 2026. Please use registration number 3015416207 when referencing this establishment in official correspondence.
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