# Stimwave Technologies Inc., Dba Stimq, LLC

- Location (FDA's records): Fort Lauderdale, FL
- FDA decisions: 1 (2017–2017): 1 510(k) clearance
- Product codes: GZF (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Stimq, LLC: 1 (https://510kreport.com/company/stimq)
- Stimwave Technologies Incorporated: 1 (https://510kreport.com/company/stimwave-technologies)

## Firms that cite its devices most
- Curonix: 1 (https://510kreport.com/company/curonix)
- Boston Scientific Neuromodulation: 1 (https://510kreport.com/company/boston-scientific-neuromodulation)
- Micron Medical Corporation: 1 (https://510kreport.com/company/micron-medical)

## Its most-cited devices
- K171366: Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, SWAG Kit, SWAG Accessory Kit, Charger Kit (2017), cited by 3

## Recent decisions
- K171366: Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, SWAG Kit, SWAG Accessory Kit, Charger Kit (Aug 4, 2017)

Source page: https://510kreport.com/company/stimwave-technologies-dba-stimq