# Ness-Neuromuscular Electrical Stimulation Systems

- Location (FDA's records): Washington, DC
- FDA decisions: 7 (2001–2011): 7 510(k) clearances
- Product codes: GZI (5), IPG (1), IPF (1)
- Predicates its devices cite: 13 (2 its own); citations of its devices by later devices: 6 (2 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
- Neuromusclar Electrical Stimulation Systems, Ltd.: 5 (https://510kreport.com/company/neuromusclar-electrical-stimulation-systems)
- N.E.S.S. Nuromuscular Electrical Stimulation Syst: 3 (https://510kreport.com/company/ness-nuromuscular-electrical-stimulation-syst)
- Dan Med, Inc.: 1 (https://510kreport.com/company/dan-med)
- Department of Medical Physics and Biomedical Eng.: 1 (https://510kreport.com/company/department-of-medical-physics-and-biomedical-eng)
- Neuromotion, Inc.: 1 (https://510kreport.com/company/neuromotion)

## Firms that cite its devices most
- Bioness, Inc.: 3 (https://510kreport.com/company/bioness)
- Otto Bock, Austria GmbH: 1 (https://510kreport.com/company/otto-bock-austria)

## Its most-cited devices
- K022776: Ness System (2002), cited by 2
- K111767: Ness H200 Wireless Hand Rehabilitation System User Kit and Clinican Kit (2011), cited by 1
- K080219: Modification to:Ness L300 (2008), cited by 1
- K053468: NESS L300 (2006), cited by 1
- K031900: Handmaster (2003), cited by 1

## Recent decisions
- K111767: Ness H200 Wireless Hand Rehabilitation System User Kit and Clinican Kit (Sep 15, 2011)
- K080219: Modification to:Ness L300 (Feb 28, 2008)
- K053468: NESS L300 (Jul 7, 2006)
- K031900: Handmaster (Aug 8, 2003)
- K024279: Ness Children System (Feb 5, 2003)
- K022776: Ness System (Sep 11, 2002)
- K012823: Modification to Handmaster (Nov 14, 2001)

Source page: https://510kreport.com/company/ness-neuromuscular-electrical-stimulation-systems