Syncthink, Inc. is one of 16306 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
Regulatory submissions have been managed by O'Connell Regulatory Consultants, Inc. and Arina Consulting, LLC.
FDA 510(k) Regulatory Record - Syncthink, Inc.
2 devices