Medical Device Manufacturer · US , St. Louis , MO

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

2 submissions · 2 cleared · Since 2020

Total

Cleared

Denied

Sentiar, Inc. has 2 FDA 510(k) cleared medical devices. Based in St. Louis, US.

Last cleared in 2023. Active since 2020. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Sentiar, Inc. Filter by specialty or product code using the sidebar.

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

2 devices

1-2 of 2