Research & Development
Pioneering next-generation surgical solutions through rigorous innovation and clinical excellence
Our Mission
NEG+ is committed to developing transformative medical devices that address critical unmet needs in women’s pelvic health and gynecologic surgery. Our research and development efforts focus on improving patient outcomes, enhancing procedural efficiency, and expanding access to minimally invasive care.
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Research Focus Areas​
Our R&D portfolio spans multiple domains of women’s surgical care, each addressing specific clinical challenges with innovative technological approaches.​
Surgical Innovation
Developing advanced surgical instrumentation and integrated energy delivery systems designed to improve precision, reduce operative time, and enhance patient safety during complex gynecologic procedures.
Diagnostic Technologies
Creating objective measurement systems that standardize clinical assessment and provide reproducible, data-driven diagnostic capabilities for pelvic floor disorders.
Procedural Efficiency
Engineering precision delivery systems that enable accurate, reproducible performance of office-based and ambulatory surgical procedures with enhanced ergonomics and reduced variability.
Minimally Invasive Approaches
Advancing laparoscopic and robotic-assisted surgical techniques through novel device designs that reduce tissue trauma, minimize complications, and accelerate patient recovery.
Data Analytics Integration
Incorporating digital health technologies and analytics platforms to support clinical decision-making, outcomes tracking, and continuous quality improvement.
Ergonomic Design
Applying human factors engineering principles to create intuitive, surgeon-friendly devices that reduce learning curves and enhance procedural reproducibility across diverse clinical settings.
Innovation Pipeline
Our development process follows rigorous, stage-gated methodology to ensure safety, efficacy, and clinical value at every milestone.
Concept Development
Clinical needs assessment, voice-of-customer research, and feasibility analysis.
Prototype Engineering
Design verification, bench testing, and iterative refinement of device concepts.
Preclinical Validation
Rigorous testing protocols including mechanical, electrical, and biocompatibility studies.
Regulatory Clearance
Comprehensive regulatory submissions and quality management system compliance.
Clinical Studies
Human factors validation and multi-center clinical trials demonstrating safety and performance.
Commercial Launch
Market introduction with ongoing post-market surveillance and continuous improvement.
Core Capabilities
Our multidisciplinary team brings together expertise across engineering, clinical medicine, regulatory science, and manufacturing to deliver innovative solutions.
Mechanical Engineering
Advanced mechanism design, precision manufacturing, and materials science expertise.
Electrosurgical Systems
Energy delivery platform integration, electrical safety testing, and thermal management.
Sensor Technology
Precision measurement systems, calibration methodologies, and signal processing algorithms.
Software Development
Embedded systems, cloud platforms, and data analytics infrastructure for connected devices.
Clinical Research
Study design, biostatistics, and evidence generation through rigorous clinical investigation.
Regulatory Affairs
FDA submission strategies, ISO compliance, and global regulatory pathway development.
Quality Management
Design controls, risk management per ISO 14971, and quality system implementation.
Manufacturing Partnership
Contract manufacturing relationships, process validation, and supply chain management.
Engagement Models
Flexible structures designed to meet your organization’s specific needs
Clinical-Driven Design
Direct surgeon input and patient outcome data guide every design decision
Evidence-Based Innovation
Rigorous preclinical and clinical testing validates safety and performance claims
Iterative Refinement
Continuous improvement through user feedback and post-market surveillance
Patient Safety First
Comprehensive risk management and failure mode analysis throughout development
Accessibility Focus
Designing solutions that can be deployed across diverse healthcare settings globally
Data-Driven Optimization
Leveraging real-world evidence to continuously enhance device performance
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Device Programs
Multiple
Patents Pending
400K +
Annual Procedures Addressable
$400M +
Market Opportunity
Intellectual Property
NEG+ maintains a robust intellectual property strategy to protect our innovations while fostering continued advancement in women’s surgical care. Our portfolio includes pending patents covering novel device architectures, energy delivery systems, measurement methodologies, and integrated surgical techniques. We are committed to responsible IP management that balances proprietary protection with the broader goal of improving patient care.
Partner With Us
We welcome collaboration with leading research institutions, clinical investigators, industry partners, and investors who share our commitment to advancing women’s health.