Vulnerability Scanning
Identifying known cybersecurity vulnerabilities across connected devices and supporting systems
Cybersecurity for medical devices is a statutory requirement across the Total Product Life Cycle under Section 524B of the Federal Food, Drug, and Cosmetic Act (FD&C Act). Manufacturers are required to establish and maintain processes to identify, assess, and address cybersecurity vulnerabilities over time.
MedSec Vulnerability Scanning helps medical device manufacturers meet these lifecycle obligations by providing expert-configured identification of known cybersecurity vulnerabilities across connected devices and supporting systems.
You've Got Options
Delivered as a one-time assessment or ongoing, recurring scans. The service offers scalable visibility into CVEs, misconfigurations, and outdated components aligned with FDA cybersecurity expectations.
Let's discuss the option that's right for you.