Sintea Plustek is one of 19178 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sintea Plustek - FDA 510(k) Cleared Devices
Recent clearances: PLIF LITE AND TLIF LITE
1
Total
1
Cleared
0
Denied
Sintea Plustek has 1 FDA 510(k) cleared medical devices. Based in Fr. Myers, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sintea Plustek Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sintea Plustek
1 devices