# Wavi Co.

- Location (FDA's records): Englewood, CO
- FDA decisions: 2 (2017–2022): 2 510(k) clearances
- Product codes: GXY (1), GWQ (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (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
- Electro-Cap Intl., Inc.: 2 (https://510kreport.com/company/electro-cap-intl)
- Evoke Neuroscience, Inc.: 1 (https://510kreport.com/company/evoke-neuroscience)
- Mitsar Co., Ltd.: 1 (https://510kreport.com/company/mitsar)
- Neuronetrix Solutions: 1 (https://510kreport.com/company/neuronetrix-solutions)

## Firms that cite its devices most
- Memory MD, Inc.: 1 (https://510kreport.com/company/memory-md)

## Its most-cited devices
- K162460: WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts (2017), cited by 1

## Recent decisions
- K213900: WAVi SCAN EEG System and Accessories (May 6, 2022)
- K162460: WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts (Apr 28, 2017)

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