Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013019295

FEI Number

3013019295

Entity Name

Grahope New Materials Technologies Inc.

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

4th Floor, 3rd building, Longcheng Industrial Park,, Huangge Community, Longcheng Street, Longgang District, Shenzhen Guangdong 518057, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Grahope New Materials Technologies Inc. (Owner Number: 10053062)

Owner / Operator Contact Address

4th Floor, 3rd building, Longcheng Industrial Park, Huangge Community, Longcheng Street, Longgang District, Shenzhen, CN-GD 518057, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SL Pure Graphene Far Infrared Heating Waist Belt SL Pure Graphene Far Infrared Heating Knee Brace SL Pure Graphene Far Infrared Heating Neck Care Device SL Pure Graphene Far Infrared Heating Nose Mask SL Pure Graphene Far Infrared Heating Music Mattress SL Pure Graphene Far Infrared Heating Pad SL Pure Graphene Far Infrared Heating Eye Mask SL Pure Graphene Far Infrared Heating Vest

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IRT	Pad, Heating, Powered	Physical Medicine	Class 2	890.5740	2016-10-27

Official Correspondent

No official correspondent registered.

US Agent Details

Manoj Zacharias Business: LIBERTY MANAGEMENT GROUP LTD. Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

Grahope New Materials Technologies Inc.

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
K881862	Thermo Body Wrap Systems, Inc.	THERMO-BODY-WRAP SYSTEM	1988-10-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013019295. Last updated year: 2026. Please use registration number 3013019295 when referencing this establishment in official correspondence.