# Ekso Bionics, Inc.

- Location (FDA's records): Richmond, CA
- FDA decisions: 4 (2016–2022): 4 510(k) clearances
- Product codes: PHL (4)
- 510(k) review time since 2016: median 86 days, against 145 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 7 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Argo Medical Technologies, Inc.: 1 (https://510kreport.com/company/argo-medical-technologies)

## Firms that cite its devices most
- Parker Hannifin Corp.: 2 (https://510kreport.com/company/parker-hannifin)
- Exoatlet Asia Co., Ltd.: 1 (https://510kreport.com/company/exoatlet-asia)
- Honda Motor Company, Ltd.: 1 (https://510kreport.com/company/honda-motor)

## Its most-cited devices
- K161443: Ekso™ (version 1.1) and Ekso GT™ (version 1.2) (2016), cited by 4
- K143690: Ekso™ (version 1.1) and Ekso GT™ (version 1.2) (2016), cited by 2
- K200574: EksoNR (2020), cited by 1

## Recent decisions
- K220988: EksoNR (Jun 9, 2022)
- K200574: EksoNR (Jun 19, 2020)
- K161443: Ekso™ (version 1.1) and Ekso GT™ (version 1.2) (Jul 19, 2016)
- K143690: Ekso™ (version 1.1) and Ekso GT™ (version 1.2) (Apr 1, 2016)

Source page: https://510kreport.com/company/ekso-bionics