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Shenzhen NearbyExpress Technology Development Company Limited

US

Last updated May 30, 2026

What Shenzhen NearbyExpress Technology Development Company Limited makes

The company manufactures transcutaneous electrical nerve stimulation (TENS) devices for pain relief, including low-frequency therapy instruments, and bioelectrical body composition analysers such as wireless smart scales that measure body metrics.

These products are classified as Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

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 Shenzhen NearbyExpress Technology Development Company Limited manufacture?

Shenzhen NearbyExpress Technology Development Company Limited specializes in two primary categories of medical devices: analgesic transcutaneous electrical nerve stimulation (TENS) systems, such as low-frequency therapy instruments designed for pain relief, and bioelectrical body composition analysers, including wireless smart scales that assess body metrics like fat, muscle, and hydration levels.

Where is Shenzhen NearbyExpress Technology Development Company Limited based?

The company is based in the United States, as indicated in its regulatory documentation. This location is relevant for understanding its operational and compliance context, particularly for devices regulated by U.S. authorities.

Which regulatory registries list devices manufactured by Shenzhen NearbyExpress Technology Development Company Limited?

Devices from this manufacturer are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is used to track and identify medical devices throughout their lifecycle, ensuring traceability and compliance with U.S. regulatory requirements.

How are the devices produced by Shenzhen NearbyExpress Technology Development Company Limited classified?

The company’s devices, including TENS systems and body composition analysers, are classified as Class II medical devices. This classification typically means they pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.

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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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
421320739

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
TAOTRONICS Wireless Body Composition Smart Scale TT-FS001
FDA UDI
Class IIActive
Low-Frequency Therapy Instrument SA-PCA008
FDA UDI
Class IIActive

Related Companies

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