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Shenzhen Longchuang Precise Electronic Technology Co., Ltd.

US

Last updated May 27, 2026

What Shenzhen Longchuang Precise Electronic Technology Co., Ltd. makes

The company manufactures hand-held electric massagers designed for muscle relaxation and pain relief, including models categorized as sleep aid therapy devices and sleep apnea therapy devices.

These devices are classified as Class I under regulatory standards 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 Longchuang Precise Electronic Technology Co., Ltd. primarily manufacture?

The company specializes in hand-held electric massagers, which are designed for muscle relaxation and pain relief. These devices are often used as sleep aid therapy devices or sleep apnea therapy devices, helping users manage discomfort or improve sleep quality through targeted stimulation.

Where is Shenzhen Longchuang Precise Electronic Technology Co., Ltd. based?

The company is headquartered in the United States. While the name includes 'Shenzhen,' the operational and regulatory presence is established within the US market.

Are Shenzhen Longchuang Precise Electronic Technology Co., Ltd.’s devices listed in any regulatory registries?

Yes, the company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices under regulatory oversight, ensuring transparency and traceability for Class I products.

How are Shenzhen Longchuang Precise Electronic Technology Co., Ltd.’s devices classified under regulatory standards?

The company’s hand-held electric massagers fall under Class I classification, which typically includes low-risk devices that pose minimal potential harm to users. This classification is determined by their intended use and design, aligning with regulatory frameworks for non-invasive, consumer-focused therapies.

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
707993428

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
SLEEP AID Therapy Devices MA1160
FDA UDI
Class IActive
Sleep Apnea Therapy Devices MA1160
FDA UDI
Class IActive

Related Companies

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