Comp Plus "T"™ LR Cuspid Roth .022

FDA UDI

Class II (US FDA UDI)

by Ortho Specialties

Identity

Trade Name: Comp Plus "T"™ LR Cuspid Roth .022 FDA UDI
Generic Name: Orthodontic bracket, plastic, single-use FDA UDI
Device Name: Lower Right Cuspid .022 Roth Rx Direct Bond Composite Orthodontic Bracket FDA UDI
Model / Reference: 710-920T FDA UDI
Description: Lower Right Cuspid .022 Roth Rx Direct Bond Composite Orthodontic Bracket FDA UDI

Identifiers

Catalog Number: 710-920T FDA UDI
Primary DI / UDI-DI: 00842452100255 FDA UDI
FDA Product Code: DYW FDA UDI
GMDN Term: Orthodontic bracket, plastic, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.5470 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic bracket, plastic, single-use

Comp Plus "T"™ LR Cuspid Roth .022 by Ortho Specialties — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic bracket, plastic, single-use.

ZENITH™ ROTH COMPOSITE BRACKETS (KIT) — G&H Wire Company, Inc. · Class II
LUCENT™ ROTH METAL LINED COMPOSITE BRACKETS — G&H Wire Company, Inc. · Class II
Silkon Plus — American Orthodontics · Class II
Carriere® Motion Pro™ — Ortho Organizers, Inc. · Class II
LUCENT™ MBT METAL LINED COMPOSITE BRACKETS — G&H Wire Company, Inc. · Class II
Silkon Plus — American Orthodontics · Class II
PRISM™ MBT COMPOSITE BRACKETS — G&H Wire Company, Inc. · Class II
PRISM™ MBT COMPOSITE BRACKETS — G&H Wire Company, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Ortho Specialties

Sources (1)

FDA UDI bdafd482-39ff-4a42-86b4-ddd4035a2a26 35 fields · synced Jun 6, 2026