Gn Resound A/S is one of 43 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Gn Resound A/S - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Gn Resound A/S has 3 FDA 510(k) cleared medical devices. Based in Ballerup, DK.
Historical record: 3 cleared submissions from 2008 to 2015. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Gn Resound A/S Filter by specialty or product code using the sidebar.
Gn Resound A/S — FDA 510(k) Products and Clearance History
3 devices
Cleared
May 14, 2015
Tinnitus Sound Generator Module
Ear, Nose, Throat
108d
Cleared
May 03, 2011
TINNITUS SOUND GENERATOR MODULE
Ear, Nose, Throat
29d
Cleared
Mar 13, 2008
TINNITUS SOUND GENERATOR MODULE
Ear, Nose, Throat
78d