Boston Endo Surgical Tech, is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Boston Endo Surgical Tech, - FDA 510(k) Cleared Devices
Recent clearances: NAV PAK Needle, NIM NAV PAK Needle, NIM PAK Needle
2
Total
2
Cleared
0
Denied
Boston Endo Surgical Tech, has 2 FDA 510(k) cleared medical devices. Based in Bridgeport, US.
Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Boston Endo Surgical Tech, Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Boston Endo Surgical Tech,
2 devices