Avertix Medical
Avertix Medical, Inc. develops innovative medical technologies, including the FDA-approved Guardian System, which is designed to detect and warn patients of acute thrombotic coronary occlusion. The company aims to improve patient outcomes by providing continuous heart monitoring and real-time alerts for high-risk patients who have experienced prior acute coronary syndrome (ACS) events, including heart attacks. Their mission is to enhance quality of life and peace of mind for heart attack survivors through advanced implantable cardiac monitoring systems.
Industries
Nr. of Employees
medium (51-250)
Avertix Medical
Products
Implantable heart attack detection and alerting system
An implantable intracardiac monitoring system that continuously samples electrical signals, detects sustained ST‑segment changes indicative of acute coronary occlusion, issues a local vibration alert to the patient and an external audible/visual alert, and stores electrogram data for clinician review.
Implantable heart attack detection and alerting system
An implantable intracardiac monitoring system that continuously samples electrical signals, detects sustained ST‑segment changes indicative of acute coronary occlusion, issues a local vibration alert to the patient and an external audible/visual alert, and stores electrogram data for clinician review.
Services
Reimbursement and coding support
Provision of coding recommendations, payer guidance, transitional pass‑through documentation, and patient prior authorization assistance to providers and facilities.
Patient education and 24/7 device support
Distribution of patient manuals, multilingual brochures and educational videos, plus a 24/7 support hotline for device-related issues.
Physician procedural resources and training materials
Provision of implant and programmer manuals, clinical procedure guidance, and clinical study documentation to support physician adoption and device programming.
Clinical study collaboration and data access
Sponsorship and sharing of clinical study designs, results, and study publications to inform clinical practice and regulatory submissions.
Reimbursement and coding support
Provision of coding recommendations, payer guidance, transitional pass‑through documentation, and patient prior authorization assistance to providers and facilities.
Patient education and 24/7 device support
Distribution of patient manuals, multilingual brochures and educational videos, plus a 24/7 support hotline for device-related issues.
Physician procedural resources and training materials
Provision of implant and programmer manuals, clinical procedure guidance, and clinical study documentation to support physician adoption and device programming.
Clinical study collaboration and data access
Sponsorship and sharing of clinical study designs, results, and study publications to inform clinical practice and regulatory submissions.
Expertise Areas
- Implantable cardiac monitoring and patient alerting
- Clinical trial design and execution for cardiac devices
- Regulatory affairs for implantable medical devices (PMA-level)
- Reimbursement strategy and coding support for novel devices
Key Technologies
- Intracardiac lead-based sensing
- Intracardiac electrogram (EGM) monitoring
- ST‑segment change detection algorithms
- Implantable medical device hardware