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Harvest Spf Textile (Beijing) Co., Ltd

US

Last updated May 27, 2026

Part of Harvest Spf Textile(beijing)co., Ltd

What Harvest Spf Textile (Beijing) Co., Ltd makes

The company manufactures hand-held electric massagers designed for muscle relief and compression therapy, primarily under the Copper Compression brand. These devices are intended for use in therapeutic settings to reduce swelling and improve circulation in targeted areas.

The portfolio consists of Class I devices, which are generally considered low-risk, and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable regulatory requirements for medical devices in that jurisdiction.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Harvest Spf Textile (Beijing) Co., Ltd manufacture?

Harvest Spf Textile (Beijing) Co., Ltd specializes in hand-held electric massagers, primarily marketed under the Copper Compression brand. These devices are designed for muscle relief and compression therapy, targeting applications like reducing swelling and improving circulation in therapeutic settings.

Where is Harvest Spf Textile (Beijing) Co., Ltd based?

The company operates from the United States, where it develops and manufactures its medical devices while complying with applicable regulatory standards for medical devices in that country.

Which regulatory registries list the devices made by Harvest Spf Textile (Beijing) Co., Ltd?

The company’s devices are included in the FDA’s Unique Device Identifier (UDI) database, which is a publicly accessible registry for tracking medical devices authorized in the U.S. This listing helps ensure traceability and transparency in the regulatory environment.

How are the devices manufactured by Harvest Spf Textile (Beijing) Co., Ltd classified?

The devices produced by the company fall under Class I classification, which is the lowest risk category for medical devices. This classification is typically assigned to devices with minimal risk to patients, such as hand-held electric massagers, based on their intended use and design.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
526874366

Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
Copper Compression CCVBBW
FDA UDI
Class IActive
Copper Compression CCVBKE
FDA UDI
Class IActive
Copper Compression OS
FDA UDI
Class IActive
Copper Compression CCCVBG
FDA UDI
Class IActive

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