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Benco

FDA UDI

Class II (US FDA UDI)

by Benco Dental Supply Co.

Identity

Trade Name
BENCO FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Natural Cure Composite 28gm FDA UDI
Model / Reference
1204-144 FDA UDI
Description
Natural Cure Composite 28gm FDA UDI

Identifiers

Primary DI / UDI-DI
00366975001146 FDA UDI
FDA Product Code
EBD FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental composite resin

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

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f18fad85-88ca-4701-bacc-3a4c0399450f 33 fields · synced Jun 6, 2026