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Garg

FDA UDI

Class I (US FDA UDI)

by Power Dental USA, Inc.

Identity

Trade Name
Garg FDA UDI
Generic Name
Dental mirror, reusable FDA UDI
Device Name
MIRROR WITH MIRROR HANDLE, MIRROR #5 C/S FRONT SURFACE WITH MIRROR HANDLE 6EZ C/S (6951+6911) FOR USE ONLY WITH POWER DENTAL USA MIRRORS / HANDLES. WE DO NOT GUARANTEE FIT OF OTHER MANUFACTURERS MIRRORS/HANDLES FDA UDI
Model / Reference
G6962 FDA UDI
Description
MIRROR WITH MIRROR HANDLE, MIRROR #5 C/S FRONT SURFACE WITH MIRROR HANDLE 6EZ C/S (6951+6911) FOR USE ONLY WITH POWER DENTAL USA MIRRORS / HANDLES. WE DO NOT GUARANTEE FIT OF OTHER MANUFACTURERS MIRRORS/HANDLES FDA UDI

Identifiers

Catalog Number
G6962 FDA UDI
Primary DI / UDI-DI
D943G69620 FDA UDI
FDA Product Code
FTX FDA UDI
GMDN Term
Dental mirror, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental mirror, reusableTumour-therapy nanoparticle suspension, magnetic hyperthermia/thermoablation

Garg by Power Dental USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tumour-therapy nanoparticle suspension, magnetic hyperthermia/thermoablation.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Power Dental USA, Inc.

Sources (1)

  • FDA UDI 1322b993-798f-44d8-b569-1b7265052627 35 fields · synced May 31, 2026