← Back to catalogue

ReVeneer Adhesive Set

FDA UDI

Class II (US FDA UDI)

by Schütz Dental GmbH

Identity

Trade Name
ReVeneer Adhesive Set FDA UDI
Generic Name
Dental repair kit, ceramic FDA UDI
Device Name
ReVeneer is an intraoral and extraoral repair system for ceramic crown and bridge veneers. FDA UDI
Model / Reference
232205 FDA UDI
Description
ReVeneer is an intraoral and extraoral repair system for ceramic crown and bridge veneers. FDA UDI

Identifiers

Primary DI / UDI-DI
ESDG2322051 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dental repair kit, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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 repair kit, ceramic

ReVeneer Adhesive Set by Schütz Dental GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental repair kit, ceramic.

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
Schütz Dental GmbH

Sources (1)

  • FDA UDI daa817c3-9682-4462-8fc0-c5cbb330bf11 34 fields · synced May 30, 2026