FDA 510(k) Applications Submitted by Ivoclar Vivadent, AG

FDA 510(k) Number Submission Date Device Name Applicant
K190272 02/08/2019 Bluephase PowerCure Ivoclar Vivadent, AG
K190339 02/14/2019 Helioseal F Plus Ivoclar Vivadent, AG
K210804 03/17/2021 Adhese Universal DC, Cention Primer Ivoclar Vivadent, AG
K191382 05/23/2019 IPS e.max CAD Abutment Solutions- extra systems Ivoclar Vivadent, AG
K191448 05/31/2019 Barrier Sleeves Ivoclar Vivadent, AG
K191453 05/31/2019 Cervitec F Ivoclar Vivadent, AG
K193193 11/19/2019 Telio CAD Abutment Solutions- extra systems Ivoclar Vivadent, AG
K163613 12/22/2016 Bluephase Style 20i IVOCLAR VIVADENT, AG
K183380 12/06/2018 Tetric PowerFill Ivoclar Vivadent, AG


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