Sintea Plastek, LLC is one of 20445 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sintea Plastek, LLC - FDA 510(k) Cleared Devices
Recent clearances: SINTEA PLUSTEK PLS MULTI-AXIAL SCREWS, DSC/ALF SPINAL SYSTEM
2
Total
2
Cleared
0
Denied
Sintea Plastek, LLC has 2 FDA 510(k) cleared medical devices. Based in Miami Beach, US.
Historical record: 2 cleared submissions from 2011 to 2012. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sintea Plastek, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sintea Plastek, LLC
2 devices