Salvin Dental Specialties is one of 18467 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Salvin Dental Specialties - FDA 510(k) Cleared Devices
Recent clearances: Salvin Tenting Screw System, Cytosurg non-resorbable PTFE Membrane, 25mm x 30mm, Cytosurg non-resorbable PTFE Membrane, 12mm x 24mm
2
Total
2
Cleared
0
Denied
Salvin Dental Specialties has 2 FDA 510(k) cleared medical devices. Based in Charlotte, US.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Salvin Dental Specialties Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Kapstone Medical and Kapstone Medical, LLC.
FDA 510(k) Regulatory Record - Salvin Dental Specialties
2 devices