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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 1 of 18
DeviceModel / ReferenceRegistriesClassStatus
Auradonics 700-330 7.5
FDA UDI
Class IActive
Auradonics 700-430 15
FDA UDI
Class IActive
Auradonics 300-404 BK
FDA UDI
Class IActive
Auradonics 700-303 15
FDA UDI
Class IActive
Auradonics 811-002NL
FDA UDI
Class IActive
Auradonics 700-519 15
FDA UDI
Class IActive
Auradonics 811-043NNL
FDA UDI
Class IActive
Auradonics 700-312 7.5
FDA UDI
Class IActive
Phoenix P-300-309
FDA UDI
Class IActive
Phoenix P-300-103
FDA UDI
Class IActive
Auradonics 811-006
FDA UDI
Class IActive
Auradonics 700-510 15
FDA UDI
Class IActive
Auradonics 700-510 7.5
FDA UDI
Class IActive
Auradonics 811-005
FDA UDI
Class IActive
Auradonics 300-429 BK
FDA UDI
Class IActive
Auradonics 300-410
FDA UDI
Class IActive
Phoenix P-700-306
FDA UDI
Class IActive
Auradonics 811-046
FDA UDI
Class IActive
Auradonics 700-625H
FDA UDI
Class IActive
Auradonics 300-401 BK
FDA UDI
Class IActive
Phoenix P-300-201
FDA UDI
Class IActive
Auradonics 811-057NL
FDA UDI
Class IActive
Phoenix P-300-214
FDA UDI
Class IActive
Auradonics 300-421 BK
FDA UDI
Class IActive
Auradonics 300-326
FDA UDI
Class IActive
Auradonics 811-058
FDA UDI
Class IActive
Auradonics 811-047
FDA UDI
Class IActive
Auradonics 811-028
FDA UDI
Class IActive
Auradonics 700-421 15
FDA UDI
Class IActive
Auradonics 700-319 15
FDA UDI
Class IActive
Phoenix P-300-102
FDA UDI
Class IActive
Auradonics 300-328
FDA UDI
Class IActive
Phoenix P-300-308
FDA UDI
Class IActive
Auradonics 700-514 15
FDA UDI
Class IActive
Auradonics 811-021
FDA UDI
Class IActive
Auradonics 811-317
FDA UDI
Class IActive
Auradonics 811-012NL
FDA UDI
Class IActive
Auradonics 300-432
FDA UDI
Class IActive
Auradonics 811-176NNL
FDA UDI
Class IActive
Auradonics 811-032NL
FDA UDI
Class IActive
Auradonics 700-318 15
FDA UDI
Class IActive
Auradonics 300-325
FDA UDI
Class IActive
Auradonics 300-110
FDA UDI
Class IActive
Auradonics 811-054
FDA UDI
Class IActive
Auradonics 500-005
FDA UDI
Class IActive
Auradonics 700-317 7.5
FDA UDI
Class IActive
Auradonics 300-301
FDA UDI
Class IActive
Auradonics 300-427
FDA UDI
Class IActive
Auradonics 700-620T
FDA UDI
Class IActive
Auradonics 700-430 7.5
FDA UDI
Class IActive

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