SUZHOU JINSHENG PLASTIC CO., LTD.

FDA Device Registration & Listing · SUZHOU Jiangsu, CN · Registration 3005245797

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
3005245797
FEI Number
3005245797
Entity Name
SUZHOU JINSHENG PLASTIC CO., LTD.
City/State/Country
SUZHOU Jiangsu, CN
Establishment Address
No.68 Xinmen Rd, Xinjia Industrial Estate, Wuzhong District, SUZHOU Jiangsu 215128, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
SUZHOU JINSHENG PLASTIC CO., LTD. (Owner Number: 9075099)
Owner / Operator Contact Address
No.68 Xinmen Rd, Xinjia Industrial Estate, Wuzhong Districy, Suzhou, CN-JS 215128, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TRIANGULAR GRADUATED GOLDEN TRANSFER TRAY Snapsecure Surgical Drape decanter device / transfer device Forceps (general / plastic surgery) Med-Stop Vacuum Control valve TRAYS light handle cover

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYW Container, Liquid Medication, Graduated General Hospital Class 1 880.6430 2005-12-20
GAZ Tubing, Noninvasive General Hospital Class 2 880.6740 2011-09-05
LRP Tray, Surgical General, Plastic Surgery Class 1 878.4800 2015-08-11
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2013-03-13
EYJ Holder, Ureteral Catheter Gastroenterology, Urology Class 1 876.5130 2021-06-01
PUI Drape, Surgical, Exempt General, Plastic Surgery Class 2 878.4370 2023-03-13
LHI Set, I.V. Fluid Transfer General Hospital Class 2 880.5440 2011-10-17
FOD Device, Occlusion, Umbilical General Hospital Class 1 880.5950 2009-01-09
GEN Forceps, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2007-06-29
FOB Bedpan General Hospital Class 1 880.6730 2016-01-11
KDP Regulator, Vacuum General Hospital Class 2 880.6740 2022-04-29
HXD Clamp General, Plastic Surgery Class 1 878.4800 2009-10-22
FTA Light, Surgical, Accessories General, Plastic Surgery Class 2 878.4580 2017-09-05
OCX Endoscopic Irrigation/Suction System Gastroenterology, Urology Class 2 876.1500 2014-02-25
EHY Tray, Impression, Preformed Dental Class 1 872.6880 2005-07-12
FNY Basin, Emesis General Hospital Class 1 880.6730 2010-02-25
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2015-12-22
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2011-09-23

Official Correspondent

No official correspondent registered.

US Agent Details

Jay Guan Email: leahxu1126@gmail.com Phone: (217) 7787707

Related Public Records

Same Entity

SUZHOU JINSHENG PLASTIC 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
K910471 Baxter Healthcare Corp MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBE 1991-03-08
K881095 CooperVision, Inc. KOI(TM) INSTRUMENT TRAYS 1988-04-06
K243985 Icu Medical, Inc. Rio™ Drug Reconstitution Transfer Device 2025-01-22
K222718 Hangzhou Qiantang Longyue Biotechnology Co., Ltd. Vial Adapter 2023-03-10
K851170 The Huxley Instrument Corp. DISSECTING TWEEZER #283-72PCS. SS 410 1985-04-25

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0036-2010 Alphatec Spine, Inc. 1
ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterilization container for ROC bolts/screws. Product is used to contain spinal implants.
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-0007-2017 Baxter Corporation Englewood 2
0.2 Micron Filter, 50 mm Product Usage: The 0.2 Micron Filter is a bacteria and particulate filter for aqueous solutions. It attaches to a standard Baxter Pharmacy Pump Tube Set.
Z-0010-2023 Hobbs Medical, Inc. 2
Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endoscopy procedures Ref: 2190
Z-0011-2023 Hobbs Medical, Inc. 2
Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 165cm Disposable For endoscopy procedures Ref: 2191

Similar Registrations

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3015916830 PACKERMAN SDN. BHD. Melaka, MY
3010692406 SHANGHAI GUANGSHENG INDUSTRIAL CO.,LTD. Shanghai, CN
1423537 Cardinal Health 200, LLC Waukegan, IL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005245797. Last updated year: 2026. Please use registration number 3005245797 when referencing this establishment in official correspondence.
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