Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022120069

FEI Number

3022120069

Entity Name

WENZHOU HONGSEN DAILY NECESSITIES, CO., LTD.

City/State/Country

Wenzhou Zhejiang, CN

Establishment Address

The west side of 104 national road, Langanqiao Village,Wanquan Town,Pingyang County, Wenzhou Zhejiang 325409, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Wenzhou Hongsen Daily Necessities, Co., Ltd. (Owner Number: 10084471)

Owner / Operator Contact Address

The west side of 104 national road, Langanqiao Village,Wanquan Town,Pingyang County, Wenzhou, CN-ZJ 325409, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Skin Pressure Sensiplast Protector

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FMP	Protector, Skin Pressure	General Hospital	Class 1	880.6450	2022-02-25

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Wenzhou Hongsen Daily Necessities, Co., Ltd.

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022120069. Last updated year: 2026. Please use registration number 3022120069 when referencing this establishment in official correspondence.