Medical Device Manufacturer · US , Berkeley , CA

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

6 submissions · 6 cleared · Since 2015

Total

Cleared

Denied

Eko Devices, Inc. has 6 FDA 510(k) cleared medical devices. Based in Berkeley, US.

Last cleared in 2023. Active since 2015. Primary specialty: Cardiovascular.

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

Regulatory submissions have been managed by Righter Consulting Group, LLC and Manatt, Phelps, & Phillips, Llp.

Eko Devices, Inc. is one of 16278 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Eko Devices, Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: May 14, 2026