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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 10 of 18
DeviceModel / ReferenceRegistriesClassStatus
Auradonics 300-331
FDA UDI
Class IActive
Auradonics 811-177NNL
FDA UDI
Class IActive
Auradonics 700-534 15
FDA UDI
Class IActive
Phoenix P-300-332
FDA UDI
Class IActive
Phoenix P-300-121
FDA UDI
Class IActive
Phoenix P-300-315
FDA UDI
Class IActive
Auradonics 700-412 15
FDA UDI
Class IActive
Auradonics 811-208NL
FDA UDI
Class IActive
Auradonics 811-015
FDA UDI
Class IActive
Auradonics 700-507 15
FDA UDI
Class IActive
Auradonics 300-416 BK
FDA UDI
Class IActive
Auradonics 811-233NNL
FDA UDI
Class IActive
Auradonics 811-179
FDA UDI
Class IActive
Auradonics 300-228
FDA UDI
Class IActive
Phoenix P-300-327
FDA UDI
Class IActive
Auradonics 600-003
FDA UDI
Class IActive
Auradonics 300-409
FDA UDI
Class IActive
Auradonics 811-024NNL
FDA UDI
Class IActive
Phoenix P-300-216
FDA UDI
Class IActive
Auradonics 300-703
FDA UDI
Class IActive
Auradonics 300-130
FDA UDI
Class IActive
Auradonics 300-100MP
FDA UDI
Class IActive
Phoenix P-700-526
FDA UDI
Class IActive
Auradonics 811-064NL
FDA UDI
Class IActive
Auradonics 700-720T
FDA UDI
Class IActive
Auradonics 700-324 7.5
FDA UDI
Class IActive
Auradonics 812-016 OSE
FDA UDI
Class IActive
Auradonics 811-055NL
FDA UDI
Class IActive
Auradonics 300-408 BK
FDA UDI
Class IActive
Auradonics 300-125
FDA UDI
Class IActive
Auradonics 300-431
FDA UDI
Class IActive
Auradonics 300-129
FDA UDI
Class IActive
Auradonics 811-315
FDA UDI
Class IActive
Phoenix P-300-205
FDA UDI
Class IActive
Auradonics 700-522 15
FDA UDI
Class IActive
Auradonics 700-516 7.5
FDA UDI
Class IActive
Auradonics 300-234
FDA UDI
Class IActive
Phoenix P-300-324
FDA UDI
Class IActive
Phoenix P-300-334
FDA UDI
Class IActive
Auradonics 811-233
FDA UDI
Class IActive
Auradonics 812-010 OSE
FDA UDI
Class IActive
Auradonics 500-004
FDA UDI
Class IActive
Auradonics 700-313 15
FDA UDI
Class IActive
Auradonics 500-008
FDA UDI
Class IActive
Auradonics 300-412
FDA UDI
Class IActive
Phoenix P-300-132
FDA UDI
Class IActive
Auradonics 812-156 OSE
FDA UDI
Class IActive
Auradonics 700-329 15
FDA UDI
Class IActive
Auradonics 811-218
FDA UDI
Class IActive
Auradonics 812-163 OSE
FDA UDI
Class IActive

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