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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
Dental matrix band retainer FDA UDI
Device Name
Tofflemire Matrix Retainer, Junior - Ca (72-30B) FDA UDI
Model / Reference
1037-432 FDA UDI
Description
Tofflemire Matrix Retainer, Junior - Ca (72-30B) FDA UDI

Identifiers

Primary DI / UDI-DI
00366975015280 FDA UDI
FDA Product Code
JEP FDA UDI
GMDN Term
Dental matrix band retainer 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental matrix band retainer

Benco by Benco Dental Supply Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental matrix band retainer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 53242765-ebab-4b02-8dc0-0172478f7f08 34 fields · synced May 30, 2026