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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
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Facebook
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
315830349

Catalogue (396)

Page 5 of 8
DeviceModel / ReferenceRegistriesClassStatus
FuturaGen Pink c 650916
FDA UDI
Class IIActive
FuturaGen Pink Opaque 650922
FDA UDI
Class IIActive
Capo Natural A 3, 4 g 232042
FDA UDI
Class IIActive
FuturAcryl 2000 Pink veined 650514
FDA UDI
Class IIActive
Nicor, 50 g 622323
FDA UDI
Class IIActive
Capo Hybrid Occlusal white, 5 g 232030
FDA UDI
Class IIActive
Capo Universal, 6 g 232054
FDA UDI
Class IIActive
Sebond Bondopaker C3 644098
FDA UDI
Class IIActive
FuturaJet Pink 650013
FDA UDI
Class IIActive
Tizian Blank Zirconia Reinforced Composite B2 220115
FDA UDI
Class IIActive
Tizian Ceramic Chroma CR-D 624882
FDA UDI
Class IIActive
Tizian Ceramic Dentin B1 624727
FDA UDI
Class IIActive
Tizian Blank Titanium Grade 2, 98 x 18 mm 624486
FDA UDI
Class IIActive
FuturaGen Pink 650923
FDA UDI
Class IIActive
NanoPaq B 3, 0.3 g 234617
FDA UDI
Class IIActive
Tizian Ceramic Chroma CR-C 624881
FDA UDI
Class IIActive
Capo Flow B 2, 2 g 234307
FDA UDI
Class IIActive
Tizian Ceramic Opaquer C4 624713
FDA UDI
Class IIActive
FuturaSelf Liquid 650662
FDA UDI
Class IIActive
Capo Bulk Fill 232060
FDA UDI
Class IIActive
Capo Natural A 1, 4 g 232040
FDA UDI
Class IIActive
Sebond Bondopaker A3 644094
FDA UDI
Class IIActive
Tresident 2000 K 212010
FDA UDI
Class IIActive
NanoPaq Flow C 3, 2 g 234721
FDA UDI
Class IIActive
Tizian Blank NEM, 98 x 18 mm 220103
FDA UDI
Class IIActive
FuturaPress LT Pink Transparent 650150
FDA UDI
Class IIActive
FuturaGen Pink Opaque Set 500 650902
FDA UDI
Class IIActive
Tizian Ceramic Glaze Fluid LG 624788
FDA UDI
Class IIActive
Tizian Ceramic Shoulder SM A 624873
FDA UDI
Class IIActive
Sebond Bondopaker B1 644096
FDA UDI
Class IIActive
Tizian Ceramic Stain Shade C 624868
FDA UDI
Class IIActive
ReVeneer Composite Filli 232231
FDA UDI
Class IIActive
Tizian Ceramic Opaque Dentin A3.5 624673
FDA UDI
Class IIActive
NanoPaq A 1, 0.3 g 234610
FDA UDI
Class IIActive
FuturaJet Pink Transparent 650020
FDA UDI
Class IIActive
Capo Natural Bleach 2, 4 g 232053
FDA UDI
Class IIActive
NanoPaq OcO, 4 g 234545
FDA UDI
Class IIActive
FuturaJet Pink Transparent 650050
FDA UDI
Class IIActive
NanoPaq IR (Incisal Red), 4 g 234547
FDA UDI
Class IIActive
EL-FORM Brightener, 100 ml 625020
FDA UDI
Class IIUnknown
FuturaPress LT Pink Transparent 650120
FDA UDI
Class IIActive
FuturaPress HP Pink IV 650426
FDA UDI
Class IIActive
NanoPaq InU, 4 g 234548
FDA UDI
Class IIActive
Tizial Ceramic Starter Set A3 624872
FDA UDI
Class IIActive
Capo Slow Flow clear, 2 g 232068
FDA UDI
Class IIActive
Capo Natural C 3, 4 g 232048
FDA UDI
Class IIActive
Tizian Ceramic Modelling Fluid LM 624784
FDA UDI
Class IIActive
Tizian Blank Titanium Grade 4, 98 x 12 mm 624488
FDA UDI
Class IIActive
NanoPaq A 3, 0.3 g 234612
FDA UDI
Class IIActive
Tizian Ceramic Opaquer C2 624711
FDA UDI
Class IIActive

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