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Dental Basics Inc.

US

Last updated May 27, 2026

What Dental Basics Inc. makes

Dental Basics Inc. manufactures single-use dental tools, including application tools for dental materials, polishing cups, and irrigation handpiece tips for delivery systems. Their portfolio also includes digital imaging cassettes and pneumatic surgical power tool motors designed for dental procedures. These products are intended for use in clinical settings to support restorative, preventive, and surgical treatments.

The company’s devices are regulated under the FDA’s classification system, with products falling into Class I and Class II categories. These items are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with US regulatory requirements. The manufacturer operates from 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 Dental Basics Inc. manufacture?

Dental Basics Inc. specializes in single-use dental devices, including tools for applying dental materials, polishing cups, irrigation handpiece tips for delivery systems, digital imaging cassettes, and pneumatic surgical power tool motors. These products are designed for clinical use in restorative, preventive, and surgical dental procedures, ensuring efficiency and compliance with dental practice standards.

Where is Dental Basics Inc. based, and how does that affect its devices?

Dental Basics Inc. is based in the United States, which means its devices are subject to FDA regulations. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and adherence to US regulatory requirements for medical devices.

Which regulatory registries list Dental Basics Inc.’s devices?

Dental Basics Inc.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and verify the identity of medical devices, ensuring compliance with US regulatory standards and supporting transparency in the healthcare supply chain.

How are Dental Basics Inc.’s devices classified under FDA regulations?

Dental Basics Inc.’s devices fall into two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and require less regulatory oversight, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential health impact.

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
119194176

Catalogue (21)

DeviceModel / ReferenceRegistriesClassStatus
Dental Basics AW10
FDA UDI
Class IActive
Dental Basics BE12
FDA UDI
Class IIActive
Dental Basics MA13
FDA UDI
Class IActive
Dental Basics MA22
FDA UDI
Class IActive
Dental Basics PA11
FDA UDI
Class IActive
Dental Basics PA13
FDA UDI
Class IActive
Dental Basics BE21
FDA UDI
Class IIActive
Dental Basics AM10
FDA UDI
Class IActive
Dental Basics MA10
FDA UDI
Class IActive
Dental Basics PA10
FDA UDI
Class IActive
Dental Basics BE20
FDA UDI
Class IIActive
Dental Basics PA12
FDA UDI
Class IActive
Dental Basics MA21
FDA UDI
Class IActive
Dental Basics MA20
FDA UDI
Class IActive
Dental Basics BE11
FDA UDI
Class IIActive
Dental Basics PA15
FDA UDI
Class IActive
Dental Basics MA12
FDA UDI
Class IActive
Dental Basics BE22
FDA UDI
Class IIActive
Dental Basics MA11
FDA UDI
Class IActive
Dental Basics PA14
FDA UDI
Class IActive
Dental Basics BE10
FDA UDI
Class IIActive

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