Satelec - Acteon, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Satelec - Acteon, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Satelec - Acteon, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mt. Laurel, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Satelec - Acteon, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Satelec - Acteon, Inc.
1 devices