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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 surgical scissors FDA UDI
Device Name
SCISSORS SUPER CUT DEAN 17.5cm FDA UDI
Model / Reference
G5907S FDA UDI
Description
SCISSORS SUPER CUT DEAN 17.5cm FDA UDI

Identifiers

Catalog Number
G5907S FDA UDI
Primary DI / UDI-DI
D943G5907S0 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Dental surgical scissors 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: General-purpose surgical scissors, reusableDental surgical scissors

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

Similar devices

Also classified as Dental surgical scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a151bf21-7df3-4b96-8eb3-1e4bea2129ef 35 fields · synced May 30, 2026