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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 8 of 18
DeviceModel / ReferenceRegistriesClassStatus
Phoenix P-700-326
FDA UDI
Class IActive
Auradonics 811-031NL
FDA UDI
Class IActive
Auradonics 811-211NL
FDA UDI
Class IActive
Auradonics 700-418 15
FDA UDI
Class IActive
Auradonics 500-006
FDA UDI
Class IActive
Auradonics 300-114
FDA UDI
Class IActive
Auradonics 700-302 15
FDA UDI
Class IActive
Phoenix P-700-328
FDA UDI
Class IActive
Auradonics 700-502 7.5
FDA UDI
Class IActive
Auradonics 700-402 7.5
FDA UDI
Class IActive
Auradonics 812-019 OSE
FDA UDI
Class IActive
Auradonics 811-318
FDA UDI
Class IActive
Auradonics 700-424 7.5
FDA UDI
Class IActive
Auradonics 700-416 7.5
FDA UDI
Class IActive
Auradonics 811-060
FDA UDI
Class IActive
Auradonics 700-405 7.5
FDA UDI
Class IActive
Auradonics 300-405 BK
FDA UDI
Class IActive
Phoenix P-300-232
FDA UDI
Class IActive
Auradonics 811-126
FDA UDI
Class IActive
Phoenix P-300-113
FDA UDI
Class IActive
Auradonics 700-433 15
FDA UDI
Class IActive
Auradonics 300-433
FDA UDI
Class IActive
Auradonics 300-400MP
FDA UDI
Class IActive
Auradonics 300-734
FDA UDI
Class IActive
Auradonics 300-233
FDA UDI
Class IActive
Auradonics 811-034NL
FDA UDI
Class IActive
Auradonics 300-108
FDA UDI
Class IActive
Auradonics 700-530 7.5
FDA UDI
Class IActive
Auradonics 811-305
FDA UDI
Class IActive
Auradonics 811-057
FDA UDI
Class IActive
Auradonics 811-222NNL
FDA UDI
Class IActive
Auradonics 700-319 7.5
FDA UDI
Class IActive
Auradonics 700-630
FDA UDI
Class IActive
Auradonics 300-400
FDA UDI
Class IActive
Auradonics 811-063
FDA UDI
Class IActive
Phoenix P-700-316
FDA UDI
Class IActive
Auradonics 700-725
FDA UDI
Class IActive
Auradonics 811-001NL
FDA UDI
Class IActive
Phoenix P-700-524
FDA UDI
Class IActive
Auradonics 811-041NNL
FDA UDI
Class IActive
Auradonics 300-320
FDA UDI
Class IActive
Auradonics 300-201 GH
FDA UDI
Class IActive
Auradonics 811-035NL
FDA UDI
Class IActive
Auradonics 700-531 15
FDA UDI
Class IActive
Auradonics 811-019
FDA UDI
Class IActive
Auradonics 300-116
FDA UDI
Class IActive
Phoenix P-300-314
FDA UDI
Class IActive
Auradonics 811-023
FDA UDI
Class IActive
Phoenix P-300-207
FDA UDI
Class IActive
Auradonics 811-301
FDA UDI
Class IActive

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