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MODERN DENTAL LABORATORY (SHENZHEN)

US

Last updated May 31, 2026

What MODERN DENTAL LABORATORY (SHENZHEN) makes

Modern Dental Laboratory (Shenzhen) manufactures mandible-repositioning sleep-disordered breathing orthoses, including The Moses appliance, designed to reposition the jaw for treatment of sleep apnea.

The company’s products are classified as Class II devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Modern Dental Laboratory (Shenzhen) manufacture?

Modern Dental Laboratory (Shenzhen) specializes in mandible-repositioning sleep-disordered breathing orthoses. These devices are specifically designed to reposition the jaw, helping treat conditions like sleep apnea. The company’s primary focus is on appliances that address sleep-related breathing disorders.

Where is Modern Dental Laboratory (Shenzhen) based?

The company is based in the United States. While the name includes 'Shenzhen,' the operational headquarters and manufacturing presence are located within the US.

Which regulatory registries or databases list Modern Dental Laboratory (Shenzhen)’s devices?

The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the US, ensuring transparency and traceability.

How are Modern Dental Laboratory (Shenzhen)’s devices classified under regulatory standards?

The devices manufactured by Modern Dental Laboratory (Shenzhen) fall under Class II classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, beyond general controls.

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
529128624

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
The Moses appliance 001
FDA UDI
Class IIActive

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