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Medical Device & IoMT Security Services

Find every connected device, contain it properly, and watch it continuously — without touching FDA-cleared firmware.

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Schedule a Device Security Call

Tell us about your device estate. We reply within 24 hours.

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Trusted by startups and global leaders

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What Is Actually Putting Your Connected Devices at Risk

Unpatched devices on your EHR network are a route to PHI.

Medical device and IoMT security monitoring across a hospital network

You Do Not Know What Is on the Network

Biomed spreadsheets go stale within weeks. Devices get plugged in, moved between wards, and never inventoried.

Devices Run Operating Systems You Cannot Patch

FDA-cleared firmware freezes the OS. Windows 7 and unsupported Linux stay in service for a decade after end-of-life.

Flat Networks Let One Device Reach Everything

A compromised ultrasound cart can talk to the EHR, PACS, and billing systems because nothing separates clinical VLANs.

Default Credentials Are Still in Place

Shared service accounts and vendor default passwords ship with the device and survive every maintenance visit.

Nobody Owns Device Security

Biomed says it is IT, IT says it is the vendor, and the vendor points at the service contract. The gap never closes.

The Numbers Behind the Medical Device Security Problem

The scale of unmanaged IoMT exposure.

How Our Medical Device Security Programme Works

We discover, segment, and monitor every device.

What You See in the Device Security Dashboard

Live inventory, risk, and behaviour for every connected device across every ward and site.

Live IoMT Asset Inventory
Make, model, firmware, and location for every device.
Device Risk & Vulnerability Heatmap
Devices ranked by CVEs, EOL OS, and PHI exposure.
Segmentation & Compliance Report
VLAN placement with audit-ready HIPAA and 524B evidence.

What Health Systems Are Seeing After Going Live

Each result traces to a specific device security gap we closed.

Book a Live Demo
3,400+
Previously unknown connected devices discovered in the first fortnight — 22% more than the biomed asset register held. — Multi-Site Hospital Group
80%
Smaller blast radius. Clinical segmentation removed every direct path from a bedside device to the EHR and PACS. — CISO, Regional Health System
70%
Faster device incident containment. Automated isolation playbooks quarantine a device without interrupting active care. — Director of Biomed Engineering
90%
Less audit preparation. Device risk registers, SBOMs, and remediation records stay continuously inspection-ready. — VP IT, Specialty Care Network

Who We Secure

For organisations where a compromised device is a patient safety event, not an IT ticket.

  • Hospitals & Multi-Site Health Systems

    Hospitals & Multi-Site Health Systems

    Hospitals & Multi-Site Health Systems

    Live inventory and segmentation across every ward, theatre, and imaging suite.

  • Medical Device Manufacturers

    Medical Device Manufacturers

    Medical Device Manufacturers

    The secure development lifecycle behind FDA 524B plans, SBOMs, and patching.

  • Imaging Centres & Diagnostic Labs

    Imaging Centres & Diagnostic Labs

    Imaging Centres & Diagnostic Labs

    PACS, DICOM, and analysers on unsupported OS, isolated properly.

  • Remote Monitoring & Digital Health Platforms

    Remote Monitoring & Digital Health Platforms

    Remote Monitoring & Digital Health Platforms

    PHI from home devices and wearables secured device to cloud.

  • Clinics & Groups Without a Security Team

    Clinics & Groups Without a Security Team

    Clinics & Groups Without a Security Team

    Managed device discovery, segmentation, and monitoring with no in-house team.

Built to the Standards That Regulators and Biomed Teams Actually Audit

Premarket obligations, postmarket monitoring, and the tooling that runs it.

Regulatory

Device Regulation

Premarket and postmarket cybersecurity obligations, handled properly.

  • FDA Section 524B
  • FDA Premarket Cybersecurity Guidance
  • EU MDR Annex I 17.2
  • IEC 81001-5-1
Compliance

Privacy & Compliance

PHI protection and audit-ready evidence across the device estate.

  • HIPAA Security Rule
  • ISO/IEC 27001
  • ISO 14971 Risk Management
  • HITRUST CSF
Discovery

IoMT Discovery

Agentless device fingerprinting that never touches cleared firmware.

  • Passive Network Fingerprinting
  • DICOM & HL7 Protocol Parsing
  • CMMS & Biomed Register Sync
  • SBOM Ingestion & Matching
Containment

Segmentation & Zero Trust

Clinical micro-segmentation that contains any single compromise.

  • Clinical VLAN Micro-Segmentation
  • NAC & 802.1X Enforcement
  • Zero Trust Device Policy
  • Automated Device Quarantine
Monitoring

Behavioural Detection

Continuous anomaly detection tuned to clinical device traffic.

  • Device Behaviour Baselining
  • Anomalous Flow Detection
  • CVE & Recall Feed Correlation
  • SIEM & SOC Integration
Coverage

Full Device Estate

Every connected class across every care setting.

  • Infusion Pumps & Ventilators
  • Imaging, PACS & Modalities
  • Patient Monitors & Telemetry
  • Lab Analysers & Remote Devices
A Compromised Infusion Pump Is Not an IT Ticket. It Is a Patient Safety Event.

Unknown devices, unpatchable firmware, and flat clinical networks cost you every day — in PHI exposure, audit findings, and risk you cannot quantify. Device security is the control that pays for itself.

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Medical Device Security Services FAQ

[ 1 ]

What are medical device security services?

Discovery, risk scoring, segmentation, and monitoring for connected clinical devices.

[ 2 ]

How is IoMT security different from standard IT security?

No agents or firmware patching on cleared devices, so passive discovery and segmentation do the work.

[ 3 ]

Will device discovery disrupt clinical operations?

No. Fingerprinting is passive, from mirrored traffic and existing DICOM, HL7, and CMMS records.

[ 4 ]

What is FDA Section 524B and does it apply to us?

Manufacturers must submit a cybersecurity plan, SBOM, and patching commitment; hospitals must monitor.

[ 5 ]

How do you secure devices running end-of-life operating systems?

Isolation: scoped clinical VLANs, allow-listed flows, NAC enforcement, behavioural monitoring.

[ 6 ]

Can you integrate with our existing CMMS and biomed asset register?

Yes. We sync and reconcile with Nuvolo, Accruent, or your CMMS so biomed and IT share one inventory.

[ 7 ]

What happens when a device is compromised or recalled?

We quarantine at the network layer and correlate recall and CVE feeds against your live inventory.

[ 8 ]

How long does a medical device security programme take to stand up?

Typically 8–12 weeks: discovery, then segmentation design, then monitoring go-live from week 8.

Global presence

Three offices. One team.

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