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Prodent Dental Technology (Shenzhen) Co., Ltd.

US

Last updated May 25, 2026

What Prodent Dental Technology (Shenzhen) Co., Ltd. makes

Prodent Dental Technology specializes in dental prosthetics, including removable partial dentures and fixed dental bridges made from ceramic and metal-ceramic materials. Their offerings are designed to restore function and aesthetics for patients requiring tooth replacement solutions.

The company’s products are classified as Class II medical devices and are listed in the FDA’s Unique Device Identification (UDI) system. Prodent Dental Technology operates with a US presence, adhering to regulatory requirements for dental prosthetics 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 Prodent Dental Technology (Shenzhen) Co., Ltd. manufacture?

Prodent Dental Technology specializes in dental prosthetics, specifically removable partial dentures and fixed dental bridges. Their bridges come in two primary forms: ceramic and metal-ceramic. These devices are designed to replace missing teeth, restoring both function and appearance for patients.

Where is Prodent Dental Technology (Shenzhen) Co., Ltd. based?

The company has a presence in the United States, where it operates in compliance with regulatory standards for dental prosthetics. While the company name includes 'Shenzhen,' its US operations are the focus for regulatory and market purposes in this region.

Which regulatory registries list Prodent Dental Technology’s devices?

Prodent Dental Technology’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry helps track and identify their dental prosthetics, ensuring traceability and compliance with US medical device regulations.

How are Prodent Dental Technology’s devices classified under medical device regulations?

Prodent Dental Technology’s dental prosthetics, including partial dentures and bridges, are classified as Class II medical devices. This classification is based on their intended use and risk level, requiring special controls beyond general controls to ensure safety and effectiveness.

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

Information

Country
US
Address
—
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
421194088

Catalogue (31)

DeviceModel / ReferenceRegistriesClassStatus
Prodent N/A
FDA UDI
Class IIActive
Prodent 160127
FDA UDI
Class IIActive
Prodent 1602203B
FDA UDI
Class IIActive
Prodent 20/40412B
FDA UDI
Class IIActive
Prodent 20/40412C
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent V12707
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent 138972
FDA UDI
Class IIActive
Prodent 20/40412B
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent 138972
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent 20/40412B
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent 16012902C
FDA UDI
Class IIActive
Prodent 160127
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive
Prodent N/A
FDA UDI
Class IIActive

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