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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 (19974)

Page 3 of 400
DeviceModel / ReferenceRegistriesClassStatus
Resin Teeth S PE / S DCL 657161
FDA UDI
Class IIActive
Tetric EvoCeram 590347WW
FDA UDI
Class IIActive
Resin Teeth DCL PE 749104
FDA UDI
Class IIActive
Resin Teeth S PE S DCL 657250
FDA UDI
Class IIActive
Resin Teeth S 657331
FDA UDI
Class IIActive
Resin Teeth S PE / S DCL 685541
FDA UDI
Class IIActive
IPS e.max ZirCAD 752152
EUDAMEDFDA UDI
Class IIActive
Resin Teeth DCL PE 565075
FDA UDI
Class IIActive
Ivostar Gnathostar 517099
FDA UDI
Class IIUnknown
SR Phonares II 645417
FDA UDI
Class IIActive
Resin Teeth S PE / S DCL 657363
FDA UDI
Class IIActive
SR Phonares II 645109
EUDAMEDFDA UDI
Class IIActive
IPS Style Ceram 673332
FDA UDI
Class IIActive
Resin Teeth S PE / S DCL 683580
FDA UDI
Class IIActive
IPS InLine 631859
EUDAMEDFDA UDI
Class IIActive
Resin Teeth / DCL / PE 608253
EUDAMEDFDA UDI
Class IIActive
IPS Style Ceram 673252
EUDAMEDFDA UDI
Class IIActive
Resin Teeth S PE / S DCL 683411
FDA UDI
Class IIActive
Resin Teeth / DCL / PE 592811
EUDAMEDFDA UDI
Class IIActive
Resin Teeth / DCL / PE 608232
FDA UDI
Class IIActive
Resin Teeth S PE / S DCL 657242
FDA UDI
Class IIActive
Resin Teeth / DCL / PE 749197
FDA UDI
Class IIActive
Resin Teeth / DCL / PE 540903
FDA UDI
Class IIUnknown
IPS Style Ceram 673345
EUDAMEDFDA UDI
Class IIActive
Resin Teeth S PE / S DCL 656785
FDA UDI
Class IIActive
Ivotion 752468
FDA UDI
Class IIActive
Resin Teeth DCL PE 523002
FDA UDI
Class IIUnknown
Adhese Universal 665156WW
FDA UDI
Class IIActive
Ivostar Gnathostar 577431
FDA UDI
Class IIActive
Resin Teeth S 646730
FDA UDI
Class IIUnknown
Resin Teeth / DCL / PE 540357
FDA UDI
Class IIActive
Resin Teeth S PE / S DCL 683538
FDA UDI
Class IIActive
Resin Teeth DCL PE 608258
FDA UDI
Class IIActive
IPS e.max ZirCAD 686894
EUDAMEDFDA UDI
Class IIActive
Resin Teeth DCL PE 564900
FDA UDI
Class IIActive
IPS e.max CAD 644364
FDA UDI
Class IIActive
IPS e.max CAD 628407
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 572274
FDA UDI
Class IIUnknown
IPS d.SIGN 563526
FDA UDI
Class IIUnknown
IPS Classic 529209
FDA UDI
Class IIUnknown
Resin Teeth DCL PE 611991
FDA UDI
Class IIUnknown
SR Ivocron 549980AN
EUDAMEDFDA UDI
Class IIActive
IPS e.max ZirCAD 752140
EUDAMEDFDA UDI
Class IIActive
Resin Teeth / DCL / PE 749431
FDA UDI
Class IIActive
Resin Teeth S PE / S DCL 683819
FDA UDI
Class IIActive
Resin Teeth DCL PE 611893
FDA UDI
Class IIUnknown
Resin Teeth S PE S DCL 683420
FDA UDI
Class IIActive
SR Phonares II 644810
FDA UDI
Class IIActive
Resin Teeth S PE S DCL 657122
FDA UDI
Class IIActive
IPS d.SIGN 556520
FDA UDI
Class IIUnknown

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