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Vitique

FDA UDI

Class II (US FDA UDI)

by DMG Chemisch-Pharmazeutische Fabrik GmbH

Identity

Trade Name
Vitique FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Water soluble glycerin-free Try-in-paste for Veneer cementation. Veneer cementation with added value. Refill: Content: 1 syringe @ 3.9 g Try-in-paste, accessories. Color: TR. FDA UDI
Model / Reference
213053 FDA UDI
Description
Water soluble glycerin-free Try-in-paste for Veneer cementation. Veneer cementation with added value. Refill: Content: 1 syringe @ 3.9 g Try-in-paste, accessories. Color: TR. FDA UDI

Identifiers

Catalog Number
213053 FDA UDI
Primary DI / UDI-DI
EDMG2130531 FDA UDI
510(k) Number
K023649 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental composite resin

Vitique by DMG Chemisch-Pharmazeutische Fabrik GmbH — 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 f828d621-92b7-4a7d-a6e1-e4e905b1d999 37 fields · synced May 30, 2026