← Back to catalogue

Camouflage

FDA UDI

Class II (US FDA UDI)

by Prismatik Dentalcraft, Inc.

Identity

Trade Name
Camouflage FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Camouflage Universal Enamel, Shade B1, 20 0.2g Capsules FDA UDI
Model / Reference
70-1151-CMU0031 FDA UDI
Description
Camouflage Universal Enamel, Shade B1, 20 0.2g Capsules FDA UDI

Identifiers

Catalog Number
70-1151-CMU0031 FDA UDI
Primary DI / UDI-DI
D745701151CMU00311 FDA UDI
510(k) Number
K133850 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 0.2 Gram FDA UDI

Category: Dental composite resin

Camouflage by Prismatik Dentalcraft, Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 77db1f61-7de2-453d-a3e5-f5e7da631a91 38 fields · synced Jun 8, 2026