Medical Device Manufacturer · US , Amherst , NY

Ivoclar Vivadent, AG - FDA 510(k) Cleared Devices

31 submissions · 31 cleared · Since 2004

Total

Cleared

Denied

Ivoclar Vivadent, AG has 31 FDA 510(k) cleared dental devices. Based in Amherst, US.

Last cleared in 2022. Active since 2004.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Ivoclar Vivadent, AG

31 devices

1-12 of 31

Cleared Jun 07, 2022

Adhese Universal DC, Cention Primer

Telio CAD Abutment Solutions- extra systems

IPS e.max CAD Abutment Solutions- extra systems

IPS e.max® Press Abutment Solutions for Viteo Base Ti

K160798 · NHA

Dental · 267d

Ivoclar Vivadent, AG - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Ivoclar Vivadent, AG

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