Novodent SA is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Novodent SA - FDA 510(k) Cleared Devices
Recent clearances: Implantswiss Dental Implant System and Implantswiss Dental Abutment System, Implantswiss Dental Implant System, Implantswiss Dental Abutment System
2
Total
2
Cleared
0
Denied
Novodent SA has 2 FDA 510(k) cleared medical devices. Based in Yverdons-Les-Bains, CH.
Historical record: 2 cleared submissions from 2018 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Novodent SA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by CardioMed Device Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Novodent SA
2 devices