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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
Periodontal curette FDA UDI
Device Name
CURETTES/UNIVERSAL COLUMBIA COL 4R/4L FDA UDI
Model / Reference
G1415 FDA UDI
Description
CURETTES/UNIVERSAL COLUMBIA COL 4R/4L FDA UDI

Identifiers

Catalog Number
G1415 FDA UDI
Primary DI / UDI-DI
D943G14150 FDA UDI
FDA Product Code
EMN FDA UDI
EMK FDA UDI
DZN FDA UDI
GMDN Term
Periodontal curette 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: Periodontal curette

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

Similar devices

Also classified as Periodontal curette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4e694fe1-7794-4750-9f2b-743c58d0e473 35 fields · synced May 31, 2026