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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
Tooth extraction forceps FDA UDI
Device Name
EXTRACTION FORCEPS F5 LOWER ANTERIOR FDA UDI
Model / Reference
G4978 FDA UDI
Description
EXTRACTION FORCEPS F5 LOWER ANTERIOR FDA UDI

Identifiers

Catalog Number
G4978 FDA UDI
Primary DI / UDI-DI
D943G49780 FDA UDI
FDA Product Code
EMG FDA UDI
GMDN Term
Tooth extraction forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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: Tooth extraction forceps

A comprehensive medical device directory listing the Garg extraction forceps dental surgical instrument.

Similar devices

Also classified as Tooth extraction forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 499014d0-afd9-441e-bd6e-178936ad07d9 35 fields · synced Jul 11, 2026