NINGBO SUNCITY PACKAGE CO.,LTD

FDA Device Registration & Listing · Ningbo Zhejiang, CN · Registration 3014267819

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
3014267819
FEI Number
3014267819
Entity Name
NINGBO SUNCITY PACKAGE CO.,LTD
City/State/Country
Ningbo Zhejiang, CN
Establishment Address
No. 277 Beihai Road, Jiangbei District, Ningbo Zhejiang 315111, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Ningbo Suncity Package Co.,Ltd (Owner Number: 10056739)
Owner / Operator Contact Address
No. 277 Beihai Road, Jiangbei District, Ningbo, CN-ZJ 315111, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Liquid Dispenser Urinal solid medication Dispenser Cast Padding Casting Tapes Plaster Bandage

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2018-01-10
FNP Urinal General Hospital Class 1 880.6730 2018-01-10
NXB Dispenser, Solid Medication Physical Medicine Class 1 890.5050 2018-01-10
ITG Bandage, Cast Physical Medicine Class 1 890.3025 2022-05-13

Official Correspondent

ChengJun Ding

US Agent Details

Mark Gordon Email: Mark.W.Gordon@outlook.com Phone: (571) 4072862

Related Public Records

Same Entity

Ningbo Suncity Package 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
K944481 Garan Scientific, Inc. THE HEART PROTECTOR 1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014267819. Last updated year: 2026. Please use registration number 3014267819 when referencing this establishment in official correspondence.
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