# Neuromotion, Inc.

- Location (FDA's records): Edmonton, Alberta, CA
- FDA decisions: 1 (1998–1998): 1 510(k) clearance
- Product codes: GZI (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 3 (0 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
- Medtronic Vascular: 2 (https://510kreport.com/company/medtronic-vascular)
- Empi: 1 (https://510kreport.com/company/empi)
- Verite: 1 (https://510kreport.com/company/verite)

## Firms that cite its devices most
- Department of Medical Physics and Biomedical Eng.: 1 (https://510kreport.com/company/department-of-medical-physics-and-biomedical-eng)
- Ness-Neuromuscular Electrical Stimulation Systems: 1 (https://510kreport.com/company/ness-neuromuscular-electrical-stimulation-systems)
- Innovative Neurotronics, Inc.: 1 (https://510kreport.com/company/innovative-neurotronics)

## Its most-cited devices
- K974514: External Functional Neuromuscular Stimulator (1998), cited by 3

## Recent decisions
- K974514: External Functional Neuromuscular Stimulator (Feb 6, 1998)

Source page: https://510kreport.com/company/neuromotion