Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Schütz Dental GmbH

US

Last updated May 23, 2026

What Schütz Dental GmbH makes

Schütz Dental GmbH manufactures dental materials for appliance fabrication, including ceramic and resin-based dentin and opaque materials, as well as dental composites and repair kits for ceramics. Their portfolio also includes polymer and metal-polymer dental bridges, dental casting alloys, and brazing alloys for dental applications.

These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of dental devices does Schütz Dental GmbH manufacture?

Schütz Dental GmbH specializes in dental materials used for appliance fabrication and restorative procedures. Their product range includes ceramic and resin-based dentin and opaque materials for dental appliances, dental composites for fillings, repair kits for ceramic restorations, and dental bridges made from polymers, metal-polymer combinations, as well as casting and brazing alloys. These materials are designed to support dental technicians and practitioners in creating durable, functional, and aesthetically pleasing dental restorations.

Where is Schütz Dental GmbH based, and what does this mean for their regulatory oversight?

Schütz Dental GmbH is based in the United States. Since their devices are regulated under FDA jurisdiction, they must comply with U.S. medical device regulations, including classification under the FDA’s risk-based system. The company’s products fall under Class II, which typically requires premarket notification (510(k)) or other regulatory pathways to demonstrate substantial equivalence to a legally marketed predicate device before commercial distribution in the U.S.

Are Schütz Dental GmbH’s devices listed in any regulatory registries, and why does this matter?

Yes, Schütz Dental GmbH’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers, regulators, and other stakeholders to quickly identify and verify the specific devices in use. Listing in the UDI database is mandatory for Class II devices in the U.S. and helps streamline recalls, post-market surveillance, and compliance efforts.

How are Schütz Dental GmbH’s dental devices classified under FDA regulations, and what does this classification imply?

All of Schütz Dental GmbH’s listed devices are classified as Class II under FDA regulations. This classification indicates that while the devices pose a moderate risk, they require special controls beyond general controls (like good manufacturing practices) to ensure safety and effectiveness. For Class II devices, manufacturers typically submit a 510(k) premarket notification to demonstrate that their device is substantially equivalent to a legally marketed predicate device, ensuring it meets applicable performance standards and regulatory requirements.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
315830349

Catalogue (396)

Page 6 of 8
DeviceModel / ReferenceRegistriesClassStatus
FuturaPress LT Liquid 650162
FDA UDI
Class IIActive
FuturAcryl 2000 Clear 650515
FDA UDI
Class IIActive
FuturaPress LT Clear 650125
FDA UDI
Class IIActive
EL-FORM Electroforming Liquid, 500 ml 625015
FDA UDI
Class IIUnknown
FuturaPress LT Clear 650115
FDA UDI
Class IIActive
Tizian Ceramic Liner 2 624793
FDA UDI
Class IIActive
Capo Hybrid Incisal Medium, 5 g 232028
FDA UDI
Class IIActive
Tizian Ceramic Dentin D2 624776
FDA UDI
Class IIActive
FuturaSelf Pink Transparent veined 650621
FDA UDI
Class IIActive
Capo Flow A 2, 2 g 234302
FDA UDI
Class IIActive
NanoPaq Flow B 3, 2 g 234717
FDA UDI
Class IIActive
FuturaPress N Liquid 650261
FDA UDI
Class IIActive
FuturAcryl 2000 Clear 650525
FDA UDI
Class IIActive
FuturaJet Pink veined 650024
FDA UDI
Class IIActive
Tizian Ceramic Stain Shade 624869
FDA UDI
Class IIActive
Micronium N10, sample 610199
FDA UDI
Class IIActive
Capo Natural Set 232055
FDA UDI
Class IIActive
FuturaJet Pink Transparent 650010
FDA UDI
Class IIActive
Tizian Ceramic Stain White 624860
FDA UDI
Class IIActive
ReVeneer Opaquer Dark 232221
FDA UDI
Class IIActive
FuturAcryl 2000 Pink Transparent veined 650511
FDA UDI
Class IIActive
NanoPaq Opakdentin B 2, 0.3 g 234633
FDA UDI
Class IIActive
Tizian Ceramic Incisal S1 624759
FDA UDI
Class IIActive
FuturaPress N Pink Transparent veined 650221
FDA UDI
Class IIActive
Tizian Ceramic Dentin A2 624764
FDA UDI
Class IIActive
Tizian Ceramic Opaque Dentin D3 624752
FDA UDI
Class IIActive
Tizian Ceramic Incisal S1 624718
FDA UDI
Class IIActive
NanoPaq A 1, 4 g 234510
FDA UDI
Class IIActive
Capo Hybrid B 3, 5 g 232025
FDA UDI
Class IIActive
Tizian Blank Titanium Grade 4, 98 x 18 mm 624489
FDA UDI
Class IIActive
Micronium N10, 1000 g 610120
FDA UDI
Class IIActive
NanoPaq Set 234500
FDA UDI
Class IIActive
Capo Flow A 1, 2 g 234301
FDA UDI
Class IIActive
Tizian Ceramic Opaquer D3 624715
FDA UDI
Class IIActive
FuturaGen Pink Transparent 650910
FDA UDI
Class IIActive
Tizian Ceramic Opaque Dentin A4 624674
FDA UDI
Class IIActive
Tizian Ceramic Dentin A3 624765
FDA UDI
Class IIActive
Sebond Pink Light 644090
FDA UDI
Class IIActive
Tizian Ceramic Intensive Opaque Dentin 624900
FDA UDI
Class IIActive
Tizian Ceramic Dentin D3 624736
FDA UDI
Class IIActive
Tizian Ceramic Opaquer B1 624706
FDA UDI
Class IIActive
Tizian Ceramic Modelling Fluid LM 624783
FDA UDI
Class IIActive
FuturaPress N Liquid 650262
FDA UDI
Class IIActive
FuturaJet Liquid 650061
FDA UDI
Class IIActive
FuturaPress N Pink Opaque 650222
FDA UDI
Class IIActive
Tizian Ceramic Transparent Orange T3 624688
FDA UDI
Class IIActive
Sebond Bondopaker A4 644095
FDA UDI
Class IIActive
Capo Hybrid A 2, 5 g 232021
FDA UDI
Class IIActive
FuturaSelf Pink Transparent 650620
FDA UDI
Class IIActive
Sebond Bondopaker D2 644099
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.