Soundcure, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Soundcure, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Soundcure, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 2 cleared submissions from 2011 to 2015. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Soundcure, Inc. Filter by specialty or product code using the sidebar.
Soundcure, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Apr 13, 2015
SoundCure Serenade Tinnitus Treatment System
Ear, Nose, Throat
90d
Cleared
Aug 24, 2011
SOUNDCURE SERENADE TINNITUS TREATMENT SYSTEM
Ear, Nose, Throat
110d