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Perfectemp®10

FDA UDI

Class II (US FDA UDI)

by Den-Mat Holdings, LLC

Identity

Trade Name
Perfectemp®10 FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
PERFECTEMP10 10mL SYR A2 FDA UDI
Model / Reference
CR1220 FDA UDI
Description
PERFECTEMP10 10mL SYR A2 FDA UDI

Identifiers

Catalog Number
CR1220 FDA UDI
Primary DI / UDI-DI
D813CR12200 FDA UDI
510(k) Number
K122039 FDA UDI
FDA Product Code
EBG FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3770 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental composite resin

Perfectemp®10 by Den-Mat Holdings, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bb99709e-4a4d-46b1-8cea-1d44f85bdf45 37 fields · synced Jun 9, 2026