# Stimq, LLC

- Location (FDA's records): Fort Lauderdale, FL
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: GZF (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: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Stimwave Technologies Incorporated: 2 (https://510kreport.com/company/stimwave-technologies)
- Medtronic Vascular: 2 (https://510kreport.com/company/medtronic-vascular)
- Advanced Neuromodulation Systems: 1 (https://510kreport.com/company/advanced-neuromodulation-systems)

## Firms that cite its devices most
- Stimwave Technologies Inc., Dba Stimq, LLC: 1 (https://510kreport.com/company/stimwave-technologies-dba-stimq)

## Its most-cited devices
- K152178: StimQ Peripheral Nerve Stimulator (PNS) System (2016), cited by 1

## Recent decisions
- K152178: StimQ Peripheral Nerve Stimulator (PNS) System (Mar 11, 2016)

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