Medical Device Manufacturer · US , Boston , MA

Syncthink, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2016

Total

Cleared

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.

FDA 510(k) cleared devices by Syncthink, Inc.

2 devices

1-2 of 2