Soliton, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Soliton, Inc. has 5 FDA 510(k) cleared medical devices. Based in Houston, US.
Last cleared in 2021. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Soliton, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Soliton, Inc.
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
May 24, 2019
Soliton Acoustic Wave Device
General & Plastic Surgery
81d