SUNDELIGHT INFANT PRODUCTS LTD.

FDA Device Registration & Listing · Guangzhou Guangdong, CN · Registration 3011322033

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
3011322033
FEI Number
3011322033
Entity Name
SUNDELIGHT INFANT PRODUCTS LTD.
City/State/Country
Guangzhou Guangdong, CN
Establishment Address
No.15,3rd Industrial Park, Dongxi Road,, Xilang, Liwan, Guangzhou, P.R. China, Guangzhou Guangdong 510385, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Sundelight Infant Products Ltd. (Owner Number: 10050727)
Owner / Operator Contact Address
No.15,3rd Industrial Park, Dongxi Road,, Xilang, Liwan, Guangzhou, P.R. China, Guangzhou, CN-GD 510385, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MEF Ring, Teething, Non-Fluid Filled Dental Class 1 872.5550 2015-12-18
FNN Nipple, Lambs Feeding General Hospital Class 1 880.5640 2016-06-27
EFW Toothbrush, Manual Dental Class 1 872.6855 2017-05-08

Official Correspondent

Jacky Chen

US Agent Details

Li Wang Business: Dr. Brown's Company Email: Li.Wang@drbrownsbaby.com Phone: (314) 4453357

Related Public Records

Same Entity

Sundelight Infant Products 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
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011322033. Last updated year: 2026. Please use registration number 3011322033 when referencing this establishment in official correspondence.
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