Dental Basics Inc.
Country not established
Dental Basics Inc. is a medical device manufacturer, with 21 devices listed in FDA GUDID (FDA Class I and II) as of 12 Nov 2026.
- Devices
- 21
Registry facts
- Registries
- FDA GUDID 21
- Device classes
- FDA Class I 15
- FDA Class II 6
- Identifiers
- DUNS 119194176
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.
Catalogue
Search and filter all 21 devicesCompany details
- DUNS number
- 119194176
Frequently asked questions
How many devices does Dental Basics Inc. have in the registry?
The registry currently lists 21 devices for Dental Basics Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dental Basics Inc.'s devices?
Among its 21 most recently registered devices, Dental Basics Inc. has devices listed in FDA GUDID (21 devices).
What risk classes do Dental Basics Inc.'s devices fall under?
Among its 21 most recently registered devices, the classes recorded for Dental Basics Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dental Basics Inc. in the registry?
The most recently registered devices listed for Dental Basics Inc. include Dental Basics AW10, Dental Basics BE12, Dental Basics MA13 and Dental Basics MA22.