Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006636962

FEI Number

3006636962

Entity Name

JIE GAO PLASTIC PRODUCTS CO., LTD.

City/State/Country

DONGGUAN CITY Guangdong, CN

Establishment Address

No.31, HuangLing Road, Cashan Town, DONGGUAN CITY Guangdong 523376, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

JIE GAO PLASTIC PRODUCTS CO., LTD. (Owner Number: 9103899)

Owner / Operator Contact Address

No.31, HuangLing Road, Cashan Town, DONGGUAN, CN-GD 523376, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Medline, Mixer, Cement, for Clinical Use - JDZ Medline, Container, Liquid Medication, Graduated - KYW MEDLINE TRAYS Medline, Tray, Surgical, Instrument - FSM MEDLINE MAYO STAND TRAYS Medline, Tray Surgical - LRP

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JDZ	Mixer, Cement, For Clinical Use	Orthopedic	Class 1	888.4210	2010-04-06
FNY	Basin, Emesis	General Hospital	Class 1	880.6730	2008-06-12
KYW	Container, Liquid Medication, Graduated	General Hospital	Class 1	880.6430	2011-09-02
CAE	Airway, Oropharyngeal, Anesthesiology	Anesthesiology	Class 1	868.5110	2019-04-22
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2007-07-05
LRP	Tray, Surgical	General, Plastic Surgery	Class 1	878.4800	2007-07-05
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2015-11-10

Official Correspondent

Lynn Chen

US Agent Details

Rosanna Lee Business: Simcon International, LLC Email: rlee@simconintl.com Phone: (847) 9492290

Related Public Records

Same Entity

JIE GAO 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
K881095	CooperVision, Inc.	KOI(TM) INSTRUMENT TRAYS	1988-04-06

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2014	King Systems Corp.	1	King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.
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-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.

Similar Registrations

Registration Number	Establishment Name	Location
3013186738	Heraeus Medical LLC	Yardley, PA, US
3033536319	MEDI.PLAN GMBH & CO. KG	Dortmund North Rhine-Westphalia, DE
3004142400	GLOBUS MEDICAL, INC.	AUDUBON, PA, US
1649518	Sterigenics US LLC	Fort Worth, TX, US
3003120897	MEDTRONIC SOFAMOR DANEK USA, INC.	Memphis, TN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006636962. Last updated year: 2026. Please use registration number 3006636962 when referencing this establishment in official correspondence.