Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016232365

FEI Number

3016232365

Entity Name

SHENZHEN FOAMTECH CO., LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Building No. 5, Minxing Industrial Park, Minzhi Area, Longhua District, Shenzhen Guangdong 518131, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Shenzhen FoamTech Co., LTD (Owner Number: 10090838)

Owner / Operator Contact Address

Building No. 5, Minxing Industrial Park, Minzhi Area, Longhua District, Shenzhen, CN-GD 518131, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Perineal Post Pad: NO001

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	2024-05-21

Official Correspondent

Wenxiong He

US Agent Details

Fanfei Liu Email: u.s.agent@frosatechnology.com Phone: (346) 7358880

Related Public Records

Same Entity

Shenzhen FoamTech 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 3016232365. Last updated year: 2026. Please use registration number 3016232365 when referencing this establishment in official correspondence.