Skip to content

3D Global Biotech, Inc.

TW Last updated 22 Oct 2026

Devices
2
Registries
FDA 510(k)FDA
FDA recalls
0

Catalogue2

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • 3D Global Biotech Inc. New Taipei City · TW FEI 3031092085

What 3D Global Biotech, Inc. makes

3D Global Biotech, Inc. manufactures orthodontic aligner systems designed for dental correction, including the DailyMate and SmileAlign systems. These products are clear, removable trays used to gradually reposition teeth without traditional braces. The systems are intended for both adult and adolescent patients seeking discreet orthodontic treatment.

The company’s orthodontic aligner systems are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) pathway. These devices are listed in the FDA’s 510(k) database, reflecting their compliance with US regulatory requirements. The company 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 3D Global Biotech, Inc. manufacture?

3D Global Biotech, Inc. specializes in orthodontic aligner systems, specifically the DailyMate and SmileAlign. These are clear, removable trays designed to gradually reposition teeth for dental correction, offering an alternative to traditional braces. They are intended for use in both adult and adolescent patients seeking discreet orthodontic treatment.

Where is 3D Global Biotech, Inc. based?

The company is headquartered in the United States. While the exact location isn’t specified, its operations and regulatory filings are conducted within the US, aligning with FDA requirements.

How are the devices manufactured by 3D Global Biotech, Inc. classified under regulatory standards?

The orthodontic aligner systems produced by 3D Global Biotech, Inc., such as the DailyMate and SmileAlign, are classified as Class II medical devices under FDA regulations. This classification applies because these devices pose a moderate risk and require special controls to ensure their safety and effectiveness, beyond general controls. The 510(k) pathway is used to demonstrate that the devices are substantially equivalent to legally marketed predicates.

Are the devices from 3D Global Biotech, Inc. listed in any regulatory registries?

Yes, the company’s orthodontic aligner systems are listed in the FDA’s 510(k) database. This registry confirms that the devices have undergone the required premarket notification process, demonstrating compliance with US regulatory requirements before being authorised for commercial distribution.

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

Information

Country
TW