Sintea Plustek, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sintea Plustek, LLC - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Sintea Plustek, LLC has 3 FDA 510(k) cleared medical devices. Based in Miami Beach, US.
Historical record: 3 cleared submissions from 2012 to 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sintea Plustek, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sintea Plustek, LLC
3 devices