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Power Dental U.S.A., Inc.

FDA UDI

Class I (US FDA UDI)

by Power Dental USA, Inc.

Identity

Trade Name
Power Dental U.S.A., Inc. FDA UDI
Generic Name
Tooth extraction forceps FDA UDI
Device Name
PREMIUM BLACK ATRAUMATIC UNIVERSAL EXTRACTION FORCEP ADULT / PEDIATRIC / CHILDREN F6P UPPER MOLARS FDA UDI
Model / Reference
N4979PB FDA UDI
Description
PREMIUM BLACK ATRAUMATIC UNIVERSAL EXTRACTION FORCEP ADULT / PEDIATRIC / CHILDREN F6P UPPER MOLARS FDA UDI

Identifiers

Catalog Number
N4979PB FDA UDI
Primary DI / UDI-DI
D943N4979PB00 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

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

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 eaa4ab33-d0d5-48e7-9021-f71528bbf9e5 35 fields · synced Jun 8, 2026