Starkey Laboratories is one of 15045 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Starkey Laboratories - FDA 510(k) Cleared Devices
Recent clearances: MULTIFLEX TINNITUS TECHNOLOGY
1
Total
1
Cleared
0
Denied
Starkey Laboratories has 1 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Starkey Laboratories 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 - Starkey Laboratories
1 devices