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Ceramage

FDA UDI

Class II (US FDA UDI)

by Shofu Dental Corp.

Identity

Trade Name
CERAMAGE FDA UDI
Generic Name
Dental prosthesis veneer resin FDA UDI
Device Name
CERAMAGE UP 2 COLOR SET FDA UDI
Model / Reference
2305 FDA UDI
Description
CERAMAGE UP 2 COLOR SET FDA UDI

Identifiers

Catalog Number
2305 FDA UDI
Primary DI / UDI-DI
E23523050 FDA UDI
510(k) Number
K162261 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental prosthesis veneer 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

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 prosthesis veneer resin

Ceramage by Shofu Dental Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis veneer resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shofu Dental Corp.

Sources (1)

  • FDA UDI 2191e8b2-f8e8-4372-a12e-2b4b1bd12660 36 fields · synced Jun 8, 2026