Sonotone Hearing Instruments is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonotone Hearing Instruments - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Sonotone Hearing Instruments has 2 FDA 510(k) cleared medical devices. Based in Longwood, US.
Historical record: 2 cleared submissions from 1992 to 1992. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Sonotone Hearing Instruments Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sonotone Hearing Instruments
2 devices