ELTON is built on frontier AI, a trusted security community, and a network of medical device engineering firms. Here is who we work with, and where the boundaries are.
Anthropic and OpenAI restrict them. ELTON holds the access.
Anthropic and OpenAI reserve their most sophisticated cyber models for verified defenders: Claude Mythos through Anthropic's Cyber Verification Program, GPT-5.6 Cyber behind Daybreak Red, the top tier of Trusted Access for Cyber. As a trusted service to medical device manufacturers, ELTON has been granted exclusive access to those models, on the strength of a verified track record and decades of service to device makers. OpenAI evaluated the ELTON service and granted Trusted Access for Cyber at the Daybreak Red tier to protect medical devices; as an OpenAI Select Partner, ELTON also works with the newest frontier models and the maximum privacy capabilities OpenAI offers. Customers get what these models find without obtaining them from Anthropic or OpenAI.
ELTON does not give customer data to these models. They decide which tools to run and write the vulnerability discovery and exploit code that the harness executes against a device. Your source code, firmware, documents and findings stay inside the pipeline. What a model sees is ELTON's own engineering work, never your product. The R&D path and the customer data path never meet.
Health-ISAC is the non-profit security community for the global health sector. As a Community Champion, ELTON gives back to its members directly.
Every Health-ISAC member is eligible for one free 510(k) or PMA FDA-Ready penetration test of a medical device: one product, tested end to end, with a submission-ready report and 30 days in the ELTON exploitability management platform. No cost, and no purchase obligation. See the member program →
Testing is one part of getting a safe device to market. These are the design, engineering, and connectivity partners we work with across the device lifecycle.
Medical device cybersecurity consulting: FDA and EU MDR compliance, security by design, penetration testing and exploitability validation, and post-market services, from first threat model through surveillance.
aktriva.com ↗
Product development for regulated products since 1982: compliant medical devices, life sciences instrumentation, digital health and regulated robotics, with systems, software and cybersecurity engineering under an ISO 13485 quality system.
fullspectrumsoftware.com ↗
End-to-end medical device design, development and contract manufacturing under one roof: human factors, electromechanical and embedded engineering, prototyping, V&V and regulatory, ISO 13485 certified.
blurpd.com ↗An out-of-the-box connectivity and digital-health platform for regulated MedTech: cloud-connected device data, managed compliance to ISO 13485, ISO 27001 and IEC 62304, and faster time to market for connected care.
kebormed.com ↗Design, development, and cyber engineering shops refer a manufacturer to ELTON, stay aligned while we test and manage, and share in recurring revenue on every renewal. The partner kit and agreements are ready to review.
If you are a manufacturer, a design firm, or a security team, there is probably a way to work together.