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Auradonics Inc.

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Auradonics Inc. is a medical device manufacturer, with 852 devices listed in FDA GUDID (FDA Class I) as of 13 Nov 2026.

Devices
852

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 852
Device classes
  • FDA Class I 852
Identifiers
  • DUNS 608537379

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.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue852

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Company details

DUNS number
608537379
Phone
8567648866

Frequently asked questions

How many devices does AURADONICS INC. have in the registry?

The registry currently lists 852 devices for AURADONICS INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list AURADONICS INC.'s devices?

Among its 50 most recently registered devices, AURADONICS INC. has devices listed in FDA GUDID (50 devices).

What risk classes do AURADONICS INC.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for AURADONICS INC.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from AURADONICS INC. in the registry?

The most recently registered devices listed for AURADONICS INC. include AURADONICS 700-330 7.5, AURADONICS 700-430 15, AURADONICS 300-404 BK and AURADONICS 700-303 15.

Generated automatically from registry data and not verified by a human reviewer.