← Back to catalogue

FuturaPress LT Pink Transparent veined

FDA UDI

Class II (US FDA UDI)

by Schütz Dental GmbH

Identity

Trade Name
FuturaPress LT Pink Transparent veined FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
Cold-curing, methyl methacrylate resinfor adding the saddles to cobalt chrome denture bases, repairs, additions and relines FDA UDI
Model / Reference
650111 FDA UDI
Description
Cold-curing, methyl methacrylate resinfor adding the saddles to cobalt chrome denture bases, repairs, additions and relines FDA UDI

Identifiers

Primary DI / UDI-DI
ESDG6501111 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 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 appliance fabrication material, resin

FuturaPress LT Pink Transparent veined by Schütz Dental GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

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 4a9d3793-a49d-45e4-b2d7-25e9998ad976 34 fields · synced Jun 8, 2026