Company

The partners behind
the proof layer.

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.

AI research

An OpenAI
Select Partner.

Frontier models are what let the pipeline write new testing tools on the fly. The partnership gives ELTON early access to those models under privacy terms built for regulated work.

OpenAI Select Partner
OpenAI · Select Partner

Bleeding-edge cyber models, with a hard data boundary.

As an OpenAI Select Partner, ELTON works with the newest frontier models and the maximum privacy capabilities OpenAI offers, and uses them for pipeline research and development: building the tools the pipeline runs and deciding which ones to run against a device.

ELTON does not send customer data directly to OpenAI. 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.

Community

A Health-ISAC
Community Champion.

Health-ISAC is the non-profit security community for the global health sector. As a Community Champion, ELTON gives back to its members directly.

Free FDA-Ready Pentest for Health-ISAC members.

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 →

Engineering & ecosystem

The medical device network
we build alongside.

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.

Aktriva
Cybersecurity design & engineering

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 ↗
Full Spectrum
Product development & engineering

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 ↗
Blur Product Development
Device design & manufacturing

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 ↗
KeborMed
Connectivity platform

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 ↗
Partner logos coming soon. These partners are shown as wordmarks pending their brand assets. Names and marks belong to their respective owners.
Work with us

Building in medical device security?

If you are a manufacturer, a design firm, or a security team, there is probably a way to work together.

Exploitability management for medical devices. FDA §524B methodologyExploitability proven at runtime95% faster than legacy testing Book a Demo
Platform
OverviewAvoid FDA DeficienciesAvoid Consulting FeesDigital Twin TraceabilityAI PentestingExploitability VerificationVulnerability ChainingRemediation OptimizationRemote TestLink™Incident ResponseAutomated VEX & MetricsCVSSv4 Migration
Solutions
Postmarket SurveillanceIncident ResponseSecurity EngineeringRegulatory AffairsFDA §524BEU MDR/CRAEU REDNIS2IMDRF N60 / N73Japan MHLW
Why ELTON
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Resources
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Company
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