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Avex CX

FDA UDI

Class I (US FDA UDI)

by Ultradent Products, Inc.

Identity

Trade Name
Avex CX FDA UDI
Generic Name
Orthodontic bracket, ceramic FDA UDI
Device Name
Avex CX .022 LL3 (0°T 3°A) FDA UDI
Model / Reference
224027 FDA UDI
Description
Avex CX .022 LL3 (0°T 3°A) FDA UDI

Identifiers

Catalog Number
224027 FDA UDI
Primary DI / UDI-DI
00883205108401 FDA UDI
FDA Product Code
EJF FDA UDI
GMDN Term
Orthodontic bracket, ceramic 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic bracket, ceramic

Avex CX by Ultradent Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic bracket, ceramic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fef397fa-5454-419d-bf79-00ace73cb368 36 fields · synced May 31, 2026