Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016914692

FEI Number

3016914692

Entity Name

JHQ NEW MATERIAL TECHNOLOGY CO., LTD.

City/State/Country

Wuxi Jiangsu, CN

Establishment Address

#203, East of zhangjing, Xigang Road, Xibei Town, Xishan Area, Wuxi Jiangsu 214194, CN

Establishment Type(s)

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

Owner / Operator

JHQ New Material Technology Co., Ltd. (Owner Number: 10090865)

Owner / Operator Contact Address

#203, East of zhangjing, Xigang Road, Xibei Town, Xishan Area, Wuxi, CN-JS 214194, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ASP Global MATTRESS, FLOTATION THERAPY, NON-POWERED

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	2024-05-30
IKY	Mattress, Flotation Therapy, Non-Powered	General Hospital	Class 1	880.5150	2024-05-24

Official Correspondent

No official correspondent registered.

US Agent Details

Emily Matorin Business: FDAbasics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

JHQ New Material Technology 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 3016914692. Last updated year: 2026. Please use registration number 3016914692 when referencing this establishment in official correspondence.