Ekso Bionics, Inc. is one of 16257 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ekso Bionics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EksoNR, EksoNR, Ekso™ (version 1.1) and Ekso GT™ (version 1.2)
4
Total
4
Cleared
0
Denied
Ekso Bionics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Richmond, US.
Last cleared in 2022. Active since 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Ekso Bionics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Ekso Bionics, Inc.
4 devices