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IVOCLAR VIVADENT AKTIENGESELLSCHAFT

US

Last updated May 23, 2026

What IVOCLAR VIVADENT AKTIENGESELLSCHAFT makes

The company manufactures resin-based artificial teeth for dental prosthetics, including preformed and custom-fit options for crowns, bridges, and veneers. It also produces ceramic and combination-material fabrication systems for dental appliances, as well as permanent dental implant suprastructures. Dental composite resins and temporary crown/bridge resins are part of its portfolio, alongside bonding agents designed for dentine adhesion.

These products are classified under FDA regulations as Class I and Class II devices, with most entries listed in the FDA’s Unique Device Identifier (UDI) database. The company’s portfolio is regulated under US medical device standards, ensuring compliance with applicable classification and reporting requirements.

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

Frequently asked questions

What types of medical devices does Ivoclar Vivadent manufacture?

Ivoclar Vivadent manufactures a range of dental devices primarily focused on restorative and prosthetic solutions. Their portfolio includes resin-based artificial teeth for crowns, bridges, and veneers, as well as ceramic and combination-material systems for dental appliance fabrication. They also produce dental composite resins, temporary crown/bridge resins, and dentine bonding agents. These products are designed to support dental prosthetics, implants, and restorative procedures.

Where is Ivoclar Vivadent based, and how does this affect their regulatory compliance?

Ivoclar Vivadent is based in the US, which means their devices are subject to FDA regulations. Since their products fall under dental categories like artificial teeth, composite resins, and bonding agents, they are classified as either Class I or Class II devices under FDA guidelines. This classification determines the regulatory pathway, including reporting requirements and compliance standards, ensuring their devices meet US medical device safety and performance criteria.

Which regulatory registries list Ivoclar Vivadent’s devices?

Ivoclar Vivadent’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices in the US, ensuring transparency in regulatory reporting and compliance. Listing in this database is common for Class I and Class II devices, as it supports traceability and adherence to FDA requirements for dental restorative and prosthetic products.

How are Ivoclar Vivadent’s devices classified under FDA regulations?

Ivoclar Vivadent’s devices are classified as either Class I or Class II under FDA regulations. Class I devices generally pose minimal risk and require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. For example, resin-based artificial teeth and bonding agents are typically Class II due to their direct interaction with patients’ oral tissues, requiring additional validation to meet regulatory standards.

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

Information

Country
US
Address
—
Website
—
LinkedIn
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Facebook
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
448015938

Catalogue (19984)

Page 12 of 400
DeviceModel / ReferenceRegistriesClassStatus
IPS Classic 531714
FDA UDI
Class IIUnknown
ProBase 531471
FDA UDI
Class IIActive
SR Phonares II 645013
FDA UDI
Class IIActive
IPS d.SIGN 560513
FDA UDI
Class IIUnknown
OptraGate Assortment 577275WW
FDA UDI
Class IActive
SR Phonares II 644969
FDA UDI
Class IIActive
IPS Style Ceram 673170
EUDAMEDFDA UDI
Class IIActive
IPS InLine 593254
EUDAMEDFDA UDI
Class IIActive
Resin Teeth S PE / S DCL 656738
FDA UDI
Class IIActive
IPS e.max Ceram 681343
EUDAMEDFDA UDI
Class IIActive
SR Phonares II 645374
FDA UDI
Class IIActive
Resin Teeth DCL PE 505082
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 504515
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 540800
FDA UDI
Class IIActive
Ivostar Gnathostar 605070
FDA UDI
Class IIActive
Resin Teeth DCL PE 540351
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 612056
FDA UDI
Class IIUnknown
IPS Classic 532109
FDA UDI
Class IIActive
Ivostar Gnathostar 577915
FDA UDI
Class IIActive
Resin Teeth S DCL 683863
FDA UDI
Class IIActive
SR Phonares II 639836
FDA UDI
Class IIActive
Resin Teeth DCL PE 592694
FDA UDI
Class IIActive
SR Phonares II 644878
FDA UDI
Class IIActive
Resin Teeth DCL PE 749490
FDA UDI
Class IIActive
Resin Teeth S DCL 683880
FDA UDI
Class IIActive
Resin Teeth / DCL / PE 540824
FDA UDI
Class IIUnknown
IPS InLine 631856
EUDAMEDFDA UDI
Class IIActive
OptraGloss 684551AN
EUDAMEDFDA UDI
Class IActive
IPS e.max ZirCAD 686282EN
FDA UDI
Class IIUnknown
IPS e.max Press 711981
FDA UDI
Class IIActive
SR Phonares II 645477
FDA UDI
Class IIActive
Resin Teeth S PE / S DCL 657192
FDA UDI
Class IIActive
Resin Teeth / DCL / PE 749477
FDA UDI
Class IIActive
IPS e.max Press 638638
EUDAMEDFDA UDI
Class IIActive
IPS e.max Ceram 596910
FDA UDI
Class IIUnknown
SR Phonares II 644858
FDA UDI
Class IIActive
Resin Teeth DCL PE 535994
FDA UDI
Class IIUnknown
Ivostar / Gnathostar 612875
FDA UDI
Class IIActive
SR Phonares II 644975
EUDAMEDFDA UDI
Class IIActive
Resin Teeth S PE / S DCL 656944
FDA UDI
Class IIActive
IPS e.max Ceram 596900
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 749605
FDA UDI
Class IIActive
Resin Teeth DCL PE 749524
FDA UDI
Class IIActive
IvoBase CAD 686182
FDA UDI
Class IIUnknown
Ivostar Gnathostar 577561
FDA UDI
Class IIActive
IPS e.max CAD 686560
FDA UDI
Class IIActive
Resin Teeth DCL PE 612225
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 505062
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 505160
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 564955
FDA UDI
Class IIActive

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