Blue Goat Cyber

Blue Goat Cyber

Speciality: Medical Device Penetration Testing

Scottsdale, United States 22 employees
[01] About

Blue Goat Cyber is a private medical equipment manufacturing company specializing in medical device cybersecurity, including penetration testing and documentation for FDA premarket submissions and post-market management; founded in 2022, with 11 employees (+120% YoY growth), headquartered in Scottsdale, Arizona, USA. The company offers full-service cybersecurity solutions for medical device manufacturers, emphasizing FDA compliance and penetration testing, and has a growing online presence with recent awards and industry leadership in MedTech cybersecurity.

Full-Service Medical Device Cybersecurity for Premarket Submissions and Postmarket Management Medical device manufacturers face immense pressure to innovate while ensuring patient safety and meeting rigorous FDA cybersecurity requirements. The complexity of these challenges can be overwhelming, with the risk of vulnerabilities threatening not just compliance but patient lives. You want to create life-saving devices that patients and healthcare providers can trust. But navigating cybersecurity requirements, building robust threat models, and preparing FDA submissions can pull focus away from your core mission. It’s easy to feel stuck, wondering if your device is truly secure and compliant. At the heart of the issue is a need for clarity, confidence, and guidance through the cybersecurity landscape. That’s where Blue Goat Cyber comes in. We specialize in helping manufacturers create secure devices that meet FDA eSTAR guidelines while protecting patient safety. Our proven processes, fixed-fee pricing, and expert support ensure that your devices are secure and compliant without disrupting your innovation. When you partner with Blue Goat Cyber, the path becomes clear. By addressing cybersecurity early, managing risks effectively, and implementing robust security measures, you can move forward with confidence. Your devices will not only meet regulatory expectations but also demonstrate your commitment to patient safety. Imagine the peace of mind that comes with knowing your devices are secure, compliant, and ready to improve lives. With Blue Goat Cyber’s guidance, you can focus on advancing technology while leaving cybersecurity challenges behind. Your reputation as a trusted innovator grows, and your patients are safer because of it. The stakes are high, but the solution is within reach. You’re building the future of healthcare—Blue Goat Cyber ensures nothing holds you back.
[02] Services
Full-service Medical Device Cybersecurity Including Penetration Testing
Risk Documentation
Threat Modeling
FDA Premarket Submission Support
Postmarket Compliance Management
Legacy Device Protection.
[03] Certifications
ISO 14971
FDA Guidance
UL 2900
AAMI TIR57
NIST 800-115
IEC 62304
ISO 13485

ISO 13485 and Cybersecurity/IT


Origin


ISO 13485 was developed by the International Organization for Standardization (ISO) and first published in 1996, with major revisions in 2003 and 2016. However, it's important to note that ISO 13485 is specifically a quality management system standard for medical devices and their related services—it is not primarily a cybersecurity or IT certification. The standard was created to help medical device manufacturers demonstrate their ability to provide devices and related services that consistently meet customer and regulatory requirements.


Industry Value


ISO 13485 is highly valued in the medical device industry because it provides a comprehensive framework for quality management that is recognized globally by regulatory authorities. Certification demonstrates an organization's commitment to product safety, regulatory compliance, and continuous improvement. While the standard itself focuses on quality management rather than cybersecurity specifically, the 2016 revision does address risk management throughout the product lifecycle, which can include cybersecurity considerations for software-based medical devices. For companies seeking to market medical devices internationally, ISO 13485 certification is often essential for regulatory approval and building customer confidence.

AAMI TIR97
ISO 27001

ISO 27001: Information Security Management Certification


Origin


ISO 27001 was developed by the International Organization for Standardization (ISO) and the International Electrotechnical Commission (IEC), and was first published in 2005. It evolved from the British Standard BS 7799-2, which was created in the late 1990s. The standard was developed in response to the growing need for organizations to systematically manage and protect sensitive information in an increasingly digital business environment. ISO 27001 has since been revised, with major updates released in 2013 and 2022 to address evolving cybersecurity threats and best practices.


Industry Value and Importance


ISO 27001 is globally recognized as the leading standard for information security management systems (ISMS) and is valued for providing a systematic, risk-based approach to protecting sensitive data. Organizations that achieve ISO 27001 certification demonstrate to clients, partners, and regulators that they have implemented comprehensive security controls and are committed to maintaining confidentiality, integrity, and availability of information. The certification is particularly important for organizations handling sensitive data, as it helps meet regulatory compliance requirements, reduces security incidents, builds customer trust, and often provides a competitive advantage in procurement processes where information security assurance is required.

IEC 81001-5-1
IEC 62443-4-1
[05] Notable Clients
  • Intuitive Surgical
  • bioMérieux
  • Nova Biomedical
  • Inogen
  • Natera