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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
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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
448015938

Catalogue (19974)

Page 7 of 400
DeviceModel / ReferenceRegistriesClassStatus
Resin Teeth / DCL / PE 749609
FDA UDI
Class IIActive
IPS d.SIGN 556510
FDA UDI
Class IIUnknown
Virtual 562855AN
FDA UDI
Class IIUnknown
Resin Teeth / DCL / PE 612695
EUDAMEDFDA UDI
Class IIActive
IPS InLine 649208
EUDAMEDFDA UDI
Class IIActive
IPS e.max ZirCAD 686935
EUDAMEDFDA UDI
Class IIActive
SR Phonares II 645069
FDA UDI
Class IIActive
IPS e.max ZirCAD 725207
EUDAMEDFDA UDI
Class IIActive
Resin Teeth S PE / S DCL 656915
FDA UDI
Class IIActive
IPS Style Ceram 673271
FDA UDI
Class IIActive
Resin Teeth S PE S DCL 657071
FDA UDI
Class IIActive
Resin Teeth S PE S DCL 657233
FDA UDI
Class IIActive
IPS InLine 593162
FDA UDI
Class IIActive
SR Phonares II 645059
FDA UDI
Class IIActive
IPS e.max Press 605288
FDA UDI
Class IIActive
Resin Teeth / DCL / PE 749630
FDA UDI
Class IIActive
IPS InLine 602933
EUDAMEDFDA UDI
Class IIActive
SR Phonares II 644830
EUDAMEDFDA UDI
Class IIActive
SR Phonares II 644911
FDA UDI
Class IIActive
Resin Teeth DCL PE 575332
FDA UDI
Class IIActive
IPS d.SIGN 556621
FDA UDI
Class IIUnknown
SR Phonares II 645047
FDA UDI
Class IIActive
IPS Style Ceram 679923AN
FDA UDI
Class IIUnknown
IPS e.max Press 626338
FDA UDI
Class IIActive
IPS Classic 529219
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 524845
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 504676
FDA UDI
Class IIUnknown
IPS Style Ceram 701570
EUDAMEDFDA UDI
Class IIActive
Resin Teeth S PE / S DCL 683734
FDA UDI
Class IIActive
Resin Teeth / DCL / PE 540490
FDA UDI
Class IIActive
IPS Ivocolor 667667
EUDAMEDFDA UDI
Class IIActive
Resin Teeth DCL PE 540607
FDA UDI
Class IIUnknown
IPS e.max CAD 605407
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 540702
FDA UDI
Class IIActive
Resin Teeth S PE S DCL 683579
FDA UDI
Class IIActive
IPS Empress CAD 665678
FDA UDI
Class IIActive
IPS e.max ZirCAD 725187
FDA UDI
Class IIActive
IvoBase 640933AN
FDA UDI
Class IIActive
Resin Teeth DCL PE 611750
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 574898
FDA UDI
Class IIActive
IPS e.max Ceram 596863
FDA UDI
Class IIUnknown
SR Nexco 640414
FDA UDI
Class IIActive
IPS InLine 602982
FDA UDI
Class IIActive
Resin Teeth S PE / S DCL 656568
FDA UDI
Class IIActive
IPS Style Ceram 673186
EUDAMEDFDA UDI
Class IIActive
Resin Teeth S PE S DCL 565887
FDA UDI
Class IIActive
Resin Teeth S 646992
FDA UDI
Class IIUnknown
Tetric EvoFlow Bulk Fill 667724WW
FDA UDI
Class IIUnknown
IPS e.max Ceram 596843
FDA UDI
Class IIActive
Resin Teeth S PE S DCL 687158
FDA UDI
Class IIActive

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