NINGBO WEIFENG HOUSEWARE CO. LTD

FDA Device Registration & Listing · Ningbo Zhejiang, CN · Registration 3033884638

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
3033884638
FEI Number
3033884638
Entity Name
NINGBO WEIFENG HOUSEWARE CO. LTD
City/State/Country
Ningbo Zhejiang, CN
Establishment Address
5F,Block A,No.307,Buzheng East Road,Jishigang Town,Haishu District, Ningbo Zhejiang 315171, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Ningbo Weifeng Houseware Co. Ltd (Owner Number: 10091826)
Owner / Operator Contact Address
5F,Block A,No.307,Buzheng East Road,Jishigang Town,Haishu District, Ningbo, CN-ZJ 315171, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TELESCOPING SELF EXAM MIRROR Wooden Footrest Roller bath brush Shaving patches for men 72pcs

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OIZ Foot Examination Tool For Inflammatory Changes Physical Medicine Class 1 890.5050 2025-09-19
LYG Massager, Therapeutic, Manual Physical Medicine Class 1 890.5660 2024-11-05
KTC Bath, Sitz, Nonpowered Physical Medicine Class 1 890.5125 2025-03-27
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2026-04-20

Official Correspondent

Sally Gong

US Agent Details

Benjamin Agredano Business: Jobar International Inc Email: b.agredano@jobar.com Phone: (310) 2228682

Related Public Records

Same Entity

Ningbo Weifeng Houseware 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 3033884638. Last updated year: 2026. Please use registration number 3033884638 when referencing this establishment in official correspondence.
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