Catheterization Lab Equipment in Wisconsin

NeuWave Medical, Inc., a wholly owned subsidiary of Quantum Surgical, Inc., specializes in developing and commercializing energy-based minimally invasive microwave ablation systems for soft tissue treatment. The company's flagship NeuWave™ Microwave Ablation System is indicated for percutaneous, open surgical, and laparoscopic-assisted ablation of non-resectable liver tumors and soft tissue lesions. The system features ABLATE-IQ™ technology for pre- and post-ablation scan fusion and margin confirmation, Tissu-Loc™ technology using CO2 cooling to minimize probe migration, and a comprehensive probe portfolio including the PRS35 probe with 35cm length for enhanced anatomical reach. The system supports multi-probe synchrony (1–3 probes) to create larger, more spherical ablation zones tailored to individual patient anatomy. Having served over 100,000 patients worldwide, NeuWave continues to pioneer microwave ablation standards and deliver clinical support through live case assistance, virtual clinical concierge services, and comprehensive procedural guidance resources.

QMD is a full-service medical device contract manufacturer specializing in silicone and elastomeric components, precision subassemblies, and finished device manufacturing. The company serves original equipment manufacturers (OEMs) across cardiology, critical care, infusion therapy, and surgical/respiratory applications. QMD's core capabilities include end-to-end manufacturing from component design through finished-device assembly, custom molded silicone and polyisoprene components (tubing, seals, valves, stoppers, duckbills), device assembly in ISO Class 7 & 8 cleanrooms, and packaging/sterilization services (ETO and gamma sterilization). Product portfolio includes coronary and peripheral vascular catheters (PTCA, PTA, aspiration), urinary catheters, enteral feeding tubes, central venous catheters, invasive blood pressure monitoring systems, chest and wound drainage products, and custom fluid management/respiratory/surgical subassemblies. The company holds FDA approvals, CE marking, 510(k) clearances, and Canadian regulatory licenses. Manufacturing capabilities span component-level customization through validated NPI processes, with private labeling and branded product transformation services. QMD operates Class 7 & 8 ISO-certified assembly facilities and provides comprehensive engineering and regulatory support to facilitate market entry for medical devices.