Soliton, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Resonic Rapid Acoustic Pulse Device, Resonic Rapid Acoustic Pulse Device, Rapid Acoustic Pulse Device
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Soliton, Inc. General & Plastic Surgery ✕
5 devices
Cleared
Nov 05, 2021
Resonic Rapid Acoustic Pulse Device
General & Plastic Surgery
88d
Cleared
Apr 27, 2021
Resonic Rapid Acoustic Pulse Device
General & Plastic Surgery
27d
Cleared
Jan 29, 2021
Rapid Acoustic Pulse Device
General & Plastic Surgery
213d
Cleared
Mar 10, 2020
Rapid Acoustic Pulse Device
General & Plastic Surgery
29d
Cleared
CT
May 24, 2019
Soliton Acoustic Wave Device
General & Plastic Surgery
81d