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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