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Auradonics

FDA UDI

Class I (US FDA UDI)

by Auradonics Inc.

Identity

Trade Name
AURADONICS FDA UDI
Generic Name
Orthodontic separator FDA UDI
Device Name
SEPO I - RADIOOPAQUE - MIDNIGHT BLUE, 960 devices per package, see www.auradonics.com FDA UDI
Model / Reference
500-002 FDA UDI
Description
SEPO I - RADIOOPAQUE - MIDNIGHT BLUE, 960 devices per package, see www.auradonics.com FDA UDI

Identifiers

Primary DI / UDI-DI
00810033832093 FDA UDI
FDA Product Code
ECI FDA UDI
GMDN Term
Orthodontic separator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic separator

Auradonics by Auradonics Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic separator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Auradonics Inc.

Sources (1)

  • FDA UDI 92b63c1e-8164-46fe-9124-0d89db7d2a3e 35 fields · synced May 29, 2026