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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 9 of 18
DeviceModel / ReferenceRegistriesClassStatus
Auradonics 811-056
FDA UDI
Class IActive
Auradonics 700-730
FDA UDI
Class IActive
Auradonics 811-212
FDA UDI
Class IActive
Auradonics 300-419 BK
FDA UDI
Class IActive
Auradonics 300-423 BK
FDA UDI
Class IActive
Auradonics 811-227
FDA UDI
Class IActive
Auradonics 811-039NL
FDA UDI
Class IActive
Auradonics 811-208
FDA UDI
Class IActive
Auradonics 811-044
FDA UDI
Class IActive
Auradonics 811-000
FDA UDI
Class IActive
Auradonics 300-424
FDA UDI
Class IActive
Auradonics 300-215 GH
FDA UDI
Class IActive
Auradonics 700-513 15
FDA UDI
Class IActive
Auradonics 700-529 7.5
FDA UDI
Class IActive
Auradonics 811-309
FDA UDI
Class IActive
Auradonics 812-022 OSE
FDA UDI
Class IActive
Auradonics 812-008 OSE
FDA UDI
Class IActive
Auradonics 811-171
FDA UDI
Class IActive
Auradonics 700-321 15
FDA UDI
Class IActive
Auradonics 700-508 15
FDA UDI
Class IActive
Auradonics 700-333 7.5
FDA UDI
Class IActive
Auradonics 812-020 OSE
FDA UDI
Class IActive
Auradonics 811-200NL
FDA UDI
Class IActive
Auradonics 700-314 15
FDA UDI
Class IActive
Auradonics 811-037
FDA UDI
Class IActive
Auradonics 700-432 15
FDA UDI
Class IActive
Auradonics 300-404
FDA UDI
Class IActive
Auradonics 811-007NL
FDA UDI
Class IActive
Auradonics 700-901
FDA UDI
Class IActive
Auradonics 300-334
FDA UDI
Class IActive
Auradonics 700-419 7.5
FDA UDI
Class IActive
Auradonics 300-121
FDA UDI
Class IActive
Phoenix P-300-101
FDA UDI
Class IActive
Auradonics 300-319
FDA UDI
Class IActive
Auradonics 700-404 7.5
FDA UDI
Class IActive
Auradonics 811-049
FDA UDI
Class IActive
Auradonics 811-035
FDA UDI
Class IActive
Auradonics 700-630T
FDA UDI
Class IActive
Auradonics 811-017
FDA UDI
Class IActive
Auradonics 811-170
FDA UDI
Class IActive
Auradonics 811-155NL
FDA UDI
Class IActive
Phoenix P-300-203
FDA UDI
Class IActive
Auradonics 811-206
FDA UDI
Class IActive
Auradonics 300-407
FDA UDI
Class IActive
Phoenix P-300-118
FDA UDI
Class IActive
Auradonics 700-428 7.5
FDA UDI
Class IActive
Auradonics 811-009NL
FDA UDI
Class IActive
Auradonics 700-504 15
FDA UDI
Class IActive
Auradonics 700-332 15
FDA UDI
Class IActive
Auradonics 811-214
FDA UDI
Class IActive

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