Syncthink, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Syncthink, Inc. has 2 FDA 510(k) cleared medical devices. Based in Boston, US.
Last cleared in 2021. Active since 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Syncthink, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Arina Consulting, LLC as regulatory consultant.
2 devices