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Mirage™ Roth Ceramic Brackets

FDA UDI

Class II (US FDA UDI)

by G&H Wire Company, Inc.

Identity

Trade Name
MIRAGE™ ROTH CERAMIC BRACKETS FDA UDI
Generic Name
Orthodontic bracket, ceramic FDA UDI
Device Name
MIRAGE™ .018 UR45 HK -7°T 0°A Mirage™ ceramic bracket system is the "clear choice" for aesthetically-minded patients. Small and smooth, with rounded corners that provide the ultimate in patient comfort, Mirage™ ceramic brackets are nearly invisible, blending inconspicuously into the oral cavity. Composed of 99.9% pure polycrystalline alumina oxide, Mirage™ ceramic brackets are impervious to stains and discoloration, helping them stay transparent for the duration of the treatment. FDA UDI
Model / Reference
60-U4-8RK-V FDA UDI
Description
MIRAGE™ .018 UR45 HK -7°T 0°A Mirage™ ceramic bracket system is the "clear choice" for aesthetically-minded patients. Small and smooth, with rounded corners that provide the ultimate in patient comfort, Mirage™ ceramic brackets are nearly invisible, blending inconspicuously into the oral cavity. Composed of 99.9% pure polycrystalline alumina oxide, Mirage™ ceramic brackets are impervious to stains and discoloration, helping them stay transparent for the duration of the treatment. FDA UDI

Identifiers

Primary DI / UDI-DI
10190886006450 FDA UDI
510(k) Number
K132368 FDA UDI
FDA Product Code
NJM FDA UDI
GMDN Term
Orthodontic bracket, ceramic 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

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

Yes

FDA UDI

Category: Orthodontic bracket, ceramic

Mirage™ Roth Ceramic Brackets by G&H Wire Company, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic bracket, ceramic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9f1338e6-5e8e-475a-94a9-a59c7dca9809 35 fields · synced Jun 8, 2026