FuturaPress HP Liquid

FDA UDI

Class II (US FDA UDI)

by Schütz Dental GmbH

Identity

Trade Name: FuturaPress HP Liquid FDA UDI
Generic Name: Dental appliance fabrication material, resin FDA UDI
Device Name: Heat-curing, methyl methacrylate resin, with liquid phase, for adding the saddles to cobalt chrome denture bases and relining dentures FDA UDI
Model / Reference: 650461 FDA UDI
Description: Heat-curing, methyl methacrylate resin, with liquid phase, for adding the saddles to cobalt chrome denture bases and relining dentures FDA UDI

Identifiers

Primary DI / UDI-DI: ESDG6504611 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental appliance fabrication material, resin

FuturaPress HP Liquid by Schütz Dental GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Schütz Dental GmbH

Sources (1)

FDA UDI b4bb9df8-6993-44ba-8c55-c90fcc9f9886 34 fields · synced Jun 8, 2026