Medical Device Manufacturer · US , Madison , WI

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

2 submissions · 2 cleared · Since 2017

Recent clearances: EnsoSleep

Total

Cleared

Denied

Ensodata, Inc. has 2 FDA 510(k) cleared medical devices. Based in Madison, US.

Last cleared in 2021. Active since 2017. Primary specialty: Neurology.

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

Ensodata, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ensodata, Inc.

2 devices

1-2 of 2