Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015532217

FEI Number

3015532217

Entity Name

RONGXING PLASTIC JURONG CO.,LTD.

City/State/Country

Zhenjiang Jiangsu, CN

Establishment Address

No.26 Chenwu market Town, Biancheng Town,Jurong City, Zhenjiang Jiangsu 212400, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Rongxing Plastic Jurong Co.,Ltd. (Owner Number: 10060798)

Owner / Operator Contact Address

No.26 Chenwu market Town, Biancheng Town,Jurong City, Zhenjiang, CN-JS 212400, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

light, surgical, accessories Container, Specimen, non-sterile Basin, Emesis Tray, Impression, Preformed Esthesiometer Instrument, Manual, Surgical, General Use Needle, Suturing, Disposable

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FTA	Light, Surgical, Accessories	General, Plastic Surgery	Class 2	878.4580	2022-06-10
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2019-06-27
FNY	Basin, Emesis	General Hospital	Class 1	880.6730	2019-06-27
EHY	Tray, Impression, Preformed	Dental	Class 1	872.6880	2019-06-27
GXB	Esthesiometer	Neurology	Class 1	882.1500	2019-06-27
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2019-06-27
GAB	Needle, Suturing, Disposable	General, Plastic Surgery	Class 1	878.4800	2019-06-27

Official Correspondent

meifen Li

US Agent Details

Min Yao Business: 9498788363 Email: yaominchina@hotmail.com Phone: (949) 8788363

Related Public Records

Same Entity

Rongxing Plastic Jurong Co.,Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015532217. Last updated year: 2026. Please use registration number 3015532217 when referencing this establishment in official correspondence.