Medical Device Manufacturer · US , Longwood , FL

Sonotone Intl., Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1992

Total

Cleared

Denied

Sonotone Intl., Inc. has 4 FDA 510(k) cleared medical devices. Based in Longwood, US.

Historical record: 4 cleared submissions from 1992 to 1992. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Sonotone Intl., Inc. Filter by specialty or product code using the sidebar.

Sonotone Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sonotone Intl., Inc.

4 devices

1-4 of 4