Unitron Hearing is one of 15045 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Unitron Hearing - FDA 510(k) Cleared Devices
Recent clearances: UNITRON TINNITUS MASKER FEATURE
1
Total
1
Cleared
0
Denied
Unitron Hearing has 1 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Unitron Hearing Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Unitron Hearing
1 devices