# Medwaves Incorporated

- Location (FDA's records): San Diego, CA
- FDA decisions: 4 (2007–2020): 4 510(k) clearances
- Names in FDA's records: Medwaves Incorporated (3); Medwaves, Inc. (1)
- Product codes: NEY (4)
- Predicates its devices cite: 10 (3 its own); citations of its devices by later devices: 3 (3 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
- Baylis Medical Co., Inc.: 1 (https://510kreport.com/company/baylis-medical)
- Neuwave Medical, Inc.: 1 (https://510kreport.com/company/neuwave-medical)
- Covidien: 1 (https://510kreport.com/company/covidien)
- Microsulis Americas, Inc.: 1 (https://510kreport.com/company/microsulis-americas)
- Radionics, Inc.: 1 (https://510kreport.com/company/radionics)
- Vivant Medical, Inc.: 1 (https://510kreport.com/company/vivant-medical)
- Valleylab, Inc.: 1 (https://510kreport.com/company/valleylab)

## Its most-cited devices
- K070356: Medwaves Microwave Coagulation/Ablation System (2007), cited by 2
- K083537: Modification to Medwaves Microwave Coagulation/Ablation System (2009), cited by 1

## Recent decisions
- K192406: AveCure BT Microwave Ablation System (Nov 25, 2020)
- K143203: AveCure Microwave Coagulation-Ablation Generator, AveCure Microwave Large Antenna-Probe, AveCure Microwave Medium Antenna-Probe, AveCure Microwave Small Antenna-Probe, AveCure Microwave Mini Antenna-Probe (Aug 26, 2015)
- K083537: Modification to Medwaves Microwave Coagulation/Ablation System (Jan 15, 2009)
- K070356: Medwaves Microwave Coagulation/Ablation System (Dec 18, 2007)

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