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Benco

FDA UDI

Class I (US FDA UDI)

by Benco Dental Supply Co.

Identity

Trade Name
BENCO FDA UDI
Generic Name
Tooth extraction forceps FDA UDI
Device Name
Crown Remover Morrell Tip C FDA UDI
Model / Reference
5094-337 FDA UDI
Description
Crown Remover Morrell Tip C FDA UDI

Identifiers

Primary DI / UDI-DI
00366975005427 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
Tooth extraction forceps 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tooth extraction forceps

Benco by Benco Dental Supply Co. — 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 70c5bbe2-7cc9-4edc-81e2-3bf2d2798168 34 fields · synced May 30, 2026