FDA 510(k) Applications Submitted by Diadent Group International

FDA 510(k) Number Submission Date Device Name Applicant
K130163 01/23/2013 D-LUX DIADENT GROUP INTERNATIONAL
K192392 09/03/2019 DiaPlus Diadent Group International
K200174 01/23/2020 DIA-ROOT BIO MTA Diadent Group International
K200175 01/23/2020 DIA-ROOT BIO Sealer Diadent Group International
K210333 02/05/2021 DiaPaste Diadent Group International
K210421 02/11/2021 Diafil & Diafil Capsule Diadent Group International
K220804 03/18/2022 Dia-X Bond Universal Diadent Group International
K200809 03/27/2020 D-LUX+ Diadent Group International
K231552 05/30/2023 Dia-Cem Diadent Group International
K192022 07/29/2019 DiaTemp Flow Diadent Group International
K192158 08/09/2019 DiaTemp Diadent Group International
K192273 08/22/2019 DIAETCH Economic Package Type A, DIATECH Regular Package, DIAETCH Refill Package Type A, DIAETCH Intro Kit Diadent Group International
K192284 08/22/2019 DiaFil Flow Diadent Group International
K192510 09/12/2019 DIAFIL & DIAFIL Capsule Diadent Group International
K213401 10/18/2021 DIAPLUS Universal Diadent Group International
K182009 07/27/2018 Dia-Proseal Diadent Group International
K190091 01/18/2019 Diapaste Diadent Group International
K182625 09/24/2018 Diapex Plus Diadent Group International


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