← Back to catalogue

Twinky Star

FDA UDI

Class II (US FDA UDI)

by VOCO GmbH

Identity

Trade Name
Twinky Star FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Coloured light-curing compmer restorative material with glitter effect. FDA UDI
Model / Reference
1683 FDA UDI
Description
Coloured light-curing compmer restorative material with glitter effect. FDA UDI

Identifiers

Catalog Number
1683 FDA UDI
Primary DI / UDI-DI
E22116831 FDA UDI
510(k) Number
K022797 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

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

Twinky Star by VOCO 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

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

Manufacturer

Manufacturer
VOCO GmbH

Sources (1)

  • FDA UDI 1d0d746c-7274-40bc-8a37-72e97ab094db 37 fields · synced May 30, 2026