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AURADONICS INC.

US

Last updated May 24, 2026

What AURADONICS INC. makes

Auradonics Inc. manufactures orthodontic accessories, including archwire/bracket ligatures, inter-arch elastic bands, inter-bracket elastic chains, and dental separators. These products are designed for use in braces and aligner treatments to apply controlled forces and maintain spacing between teeth.

The company’s portfolio consists of Class I medical devices, all listed in the FDA’s Unique Device Identification (UDI) system. The products are regulated under U.S. FDA requirements and are 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 Auradonics Inc. manufacture?

Auradonics Inc. specializes in orthodontic accessories, including archwire/bracket ligatures, inter-arch elastic bands, inter-bracket elastic chains, and dental separators. These devices are primarily used in braces and aligner treatments to help apply gentle, controlled forces or maintain proper tooth spacing during orthodontic care.

Where is Auradonics Inc. based, and how does that affect its regulatory oversight?

Auradonics Inc. is based in the United States. Since it operates within the U.S., its devices are subject to FDA regulations. The company’s products are classified as Class I medical devices, which are generally considered low-risk but still require compliance with FDA requirements, including listing in the FDA’s Unique Device Identification (UDI) system.

Are Auradonics Inc.’s devices listed in any regulatory registries, and why does this matter?

Yes, Auradonics Inc.’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry helps ensure traceability and transparency in the medical device supply chain, allowing healthcare providers, regulators, and patients to verify the identity of the device and its manufacturer. Listing in the UDI system is a requirement for Class I devices in the U.S.

How are Auradonics Inc.’s devices classified under FDA regulations, and what does that classification mean?

Auradonics Inc.’s devices are classified as Class I medical devices by the FDA. This classification is assigned based on the risk associated with the device—Class I devices are generally considered the lowest risk, often involving minimal potential harm to the user. While they still require compliance with FDA requirements, such as proper labeling and manufacturing controls, they do not undergo the same rigorous pre-market review as higher-risk devices.

What kinds of orthodontic treatments are Auradonics Inc.’s devices designed to support?

Auradonics Inc.’s devices are designed to support traditional braces and aligner treatments. The archwire/bracket ligatures and elastic chains help secure components of braces, while inter-arch elastic bands and separators apply controlled forces to move teeth or maintain spacing. These accessories are integral to achieving precise orthodontic outcomes during treatment.

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

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Phone
8567648866
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
608537379

Catalogue (852)

Page 13 of 18
DeviceModel / ReferenceRegistriesClassStatus
Auradonics 300-731
FDA UDI
Class IActive
Auradonics 300-402
FDA UDI
Class IActive
Auradonics 300-133
FDA UDI
Class IActive
Auradonics 811-212NL
FDA UDI
Class IActive
Auradonics 300-226
FDA UDI
Class IActive
Auradonics 700-525 15
FDA UDI
Class IActive
Auradonics 300-501
FDA UDI
Class IActive
Auradonics 812-024 OSE
FDA UDI
Class IActive
Phoenix P-300-226
FDA UDI
Class IActive
Auradonics 300-310
FDA UDI
Class IActive
Auradonics 300-126
FDA UDI
Class IActive
Auradonics 811-021 BLK
FDA UDI
Class IActive
Auradonics 811-203
FDA UDI
Class IActive
Auradonics 811-174
FDA UDI
Class IActive
Auradonics 700-320 7.5
FDA UDI
Class IActive
Auradonics 300-205
FDA UDI
Class IActive
Auradonics 811-312
FDA UDI
Class IActive
Auradonics 300-406
FDA UDI
Class IActive
Auradonics 700-406 15
FDA UDI
Class IActive
Phoenix P-700-528
FDA UDI
Class IActive
Auradonics 812-005 OSE
FDA UDI
Class IActive
Phoenix P-700-332
FDA UDI
Class IActive
Auradonics 811-215
FDA UDI
Class IActive
Phoenix P-300-127
FDA UDI
Class IActive
Auradonics 811-177
FDA UDI
Class IActive
Auradonics 300-113
FDA UDI
Class IActive
Auradonics 500-002
FDA UDI
Class IActive
Auradonics 811-058NL
FDA UDI
Class IActive
Auradonics 300-200MP
FDA UDI
Class IActive
Auradonics 300-224
FDA UDI
Class IActive
Auradonics 811-224
FDA UDI
Class IActive
Auradonics 700-404 15
FDA UDI
Class IActive
Auradonics 700-530 15
FDA UDI
Class IActive
Auradonics 300-709
FDA UDI
Class IActive
Auradonics 811-025
FDA UDI
Class IActive
Auradonics 811-221NNL
FDA UDI
Class IActive
Auradonics 700-515 15
FDA UDI
Class IActive
Auradonics 700-334 15
FDA UDI
Class IActive
Auradonics 700-631
FDA UDI
Class IActive
Auradonics 700-523 15
FDA UDI
Class IActive
Auradonics 300-707
FDA UDI
Class IActive
Auradonics 811-030
FDA UDI
Class IActive
Auradonics 700-405 15
FDA UDI
Class IActive
Auradonics 811-029
FDA UDI
Class IActive
Auradonics 812-001 OSE
FDA UDI
Class IActive
Auradonics 700-406 7.5
FDA UDI
Class IActive
Auradonics 700-329 7.5
FDA UDI
Class IActive
Auradonics 811-313
FDA UDI
Class IActive
Auradonics 811-206NL
FDA UDI
Class IActive
Auradonics 700-414 7.5
FDA UDI
Class IActive

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