Sonendo, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonendo, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Sonendo Filling Material 5C, GentleWave X, Sonendo GentleWave System
9
Total
9
Cleared
0
Denied
Sonendo, Inc. has 9 FDA 510(k) cleared medical devices. Based in Laguna Hills, US.
Last cleared in 2021. Active since 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sonendo, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sonendo, Inc.
9 devices
Cleared
Aug 27, 2021
Sonendo Filling Material 5C
Dental
60d
Cleared
Feb 05, 2021
GentleWave X
Dental
88d
Cleared
Mar 16, 2019
Sonendo GentleWave System
Dental
29d
Cleared
Oct 22, 2018
Sonendo Material A
Dental
96d
Cleared
Jun 03, 2016
Sonendo GentleWave System
Dental
63d
Cleared
Jan 29, 2016
Sonendo Gentle Wave System
Dental
88d
Cleared
May 01, 2015
Sonendo GentleWave System
Dental
150d
Cleared
May 15, 2014
SONENDO OMNICLEAN ENDOTHERPAY SYSTEM CONSOLE, SONENDO OMNICLEAN MOLAR...
Dental
157d
Cleared
Jun 11, 2013
SONENDO ENDOTHERAPY SYSTEM
Dental
159d