Synapse Dental is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synapse Dental - FDA 510(k) Cleared Devices
Recent clearances: Dental Pain Eraser, Dental Pain Eraser
2
Total
2
Cleared
0
Denied
Synapse Dental has 2 FDA 510(k) cleared medical devices. Based in Cranston, US.
Historical record: 2 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Synapse Dental Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Synapse Dental
2 devices