How does ORDR discover medical devices without agents or active scanning?

ORDR uses passive network traffic analysis to identify and profile medical devices based on how they communicate on the network — without installing software on devices or sending any traffic that could affect their operation. This works safely for infusion pumps, imaging systems, patient monitors, and other clinical equipment that cannot support agents and cannot tolerate active scanning.

Will segmentation policies disrupt clinical workflows or patient care?

No. ORDR validates every segmentation policy against real clinical network traffic before enforcement. You see exactly which communication flows a policy would affect — including care-critical device interactions — so you can confirm safety before any policy is applied. Patient safety is never compromised for security.

How does ORDR help with HIPAA compliance for connected medical devices?

ORDR continuously monitors all connected devices and maps control status to HIPAA Security Rule requirements — including access controls, audit logging, integrity protections, and transmission security. This provides always-current compliance evidence and gap identification without manual assessment work.

Can ORDR identify devices with FDA recalls or known vulnerabilities?

Yes. ORDR enriches device records with FDA recall status, CVE data matched to device firmware and software versions, and manufacturer security advisories. This gives clinical engineering and security teams a prioritized view of which devices have the highest risk — with compensating control recommendations for devices that can't be patched.

How does ORDR integrate with existing hospital IT and security systems?

ORDR integrates with SIEM, CMDB, ITSM, and biomedical asset management platforms via API — enriching existing workflows with clinical device context. It also connects with NAC and firewall infrastructure to enforce policies through controls you already have, without requiring new infrastructure.

Medical Device Security

Secure Every Device.
Protect Every Patient.

ORDR delivers complete visibility and protection for connected medical devices — without agents, without disruption to care delivery, and without compromising patient safety.

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15,000+

Connected medical devices in the average large hospital

78%

Of medical devices run end-of-life OS

270 days

Average attacker dwell time before detection

Agentless IoMT Discovery

Infusion pumps, imaging, monitors, and more

Clinical-Safe Segmentation

Validated against care workflows before enforcement

HIPAA Compliance Support

Continuous evidence generation

The Challenge

Connected Devices Are the New Clinical Risk

Healthcare delivers care through networks of connected devices that were never designed with cybersecurity in mind. Infusion pumps, imaging systems, patient monitors, and clinical workstations are mission-critical — and most are invisible to standard security tools.

Traditional IT security tools either can't see these devices or can't interact with them safely. The result is a massive, unmonitored attack surface in the most sensitive possible environment — where a breach doesn't just cost money, it endangers patients.

Threat Type	Impact on Healthcare	Why It's Critical
Ransomware targeting clinical systems	Encrypts EHR systems, imaging infrastructure, and connected devices — halting care delivery and forcing costly manual workarounds	Healthcare is the most targeted sector for ransomware, with average recovery costs exceeding $10M per incident
Unmanaged IoMT attack surface	The average hospital has 10–15 connected devices per bed — most unmanaged, unmonitored, and running legacy firmware	Most clinical devices can't run agents and can't tolerate active scanning, leaving them invisible to traditional security tools
Legacy OS and unpatched medical devices	78% of connected medical devices run end-of-life operating systems that can't receive security patches	Known vulnerabilities on unpatched devices are actively exploited — and device manufacturers often can't provide timely fixes
Lateral movement to clinical networks	A compromised workstation or imaging system can provide an attacker path to patient monitors, infusion pumps, and critical clinical systems	Clinical networks aren't segmented from enterprise IT in most hospitals — one breach can reach patient-safety devices
HIPAA compliance gaps	Missing controls on ePHI-adjacent systems, insufficient access monitoring, and incomplete risk assessments create regulatory exposure	HHS OCR fines for HIPAA violations have exceeded $100M in recent years — and audits can follow any breach

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Explore a sandbox environment powered by real device data. Ask ORDR IQ anything, and watch it reason across assets, surface risks, and recommend action. No commitment, no setup, no sales call.

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How ORDR Secures Medical Devices

Built for Clinical Environments

Every capability designed around the reality of healthcare delivery — where security must never compromise care.

Agentless IoMT Discovery

Passively identifies every connected medical device — infusion pumps, imaging systems, patient monitors, ventilators — without agents or scanning

Business Value

Complete clinical device inventory with zero risk to patient safety or device stability

Clinical Context & Risk Enrichment

Correlates devices with FDA recall status, CVE data, manufacturer advisories, and SBOM information for medical device-aware risk scoring

Business Value

Risk prioritization that reflects clinical impact, not just technical severity scores

Behavioral Threat Detection

Establishes communication baselines for clinical devices and alerts on anomalies — unusual destinations, protocol changes, and unexpected peer connections

Business Value

Early threat detection that doesn't disrupt care delivery or device function

Safe Network Segmentation

Generates and validates segmentation policies for clinical networks — isolating high-risk devices while preserving the communication workflows care delivery requires

Business Value

Enforce Zero Trust in clinical environments without risking patient safety or interrupting care

HIPAA-Ready Compliance Documentation

Continuously maps device controls and gaps to HIPAA Security Rule requirements with audit-ready evidence generation

Business Value

Compliance documentation that's always current — not assembled the week before an audit

FDA Cybersecurity Guidance Alignment

Supports documentation and control requirements aligned with FDA premarket and postmarket cybersecurity guidance for connected medical devices

Business Value

Security practices aligned with FDA expectations for healthcare delivery organizations

Why ORDR

Why Healthcare Organizations Choose ORDR

Patient Safety First — Always

Every security control is validated against clinical workflows before enforcement. ORDR never compromises care delivery for security — the two are designed to coexist.

See Every Connected Device

ORDR discovers the complete clinical device inventory — including shadow IT, unregistered IoMT, and legacy equipment — without touching devices or disrupting operations.

Stop Threats Before They Reach Clinical Systems

Behavioral detection identifies anomalies on clinical networks and contains threats before they can reach patient-facing devices or ePHI systems.

HIPAA Compliance That Doesn't Wait for an Audit

Continuous control monitoring maps to HIPAA Security Rule requirements with always-current evidence — so audit preparation is continuous, not a crisis.

Understands Medical Devices Natively

ORDR's clinical intelligence includes FDA recall status, SBOM data, manufacturer advisories, and IoMT-specific vulnerability enrichment that generic IT tools don't have.

No Agents. No Disruption. No Clinical Risk.

Passive deployment with no software installed on clinical devices and no active scanning that could affect device operation. Visibility achieved without touching a single medical device.

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What's the cost of a healthcare breach in your environment?

Healthcare breaches average over $10M per incident. The ORDR ROI Calculator helps quantify the financial impact of securing connected medical devices — and the savings from prevention vs. response.

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Compliance

HIPAA Security Rule Requirements

ORDR maps continuously to HIPAA Security Rule requirements — providing audit-ready evidence for controls that must be maintained on all ePHI-adjacent systems, including connected medical devices.

Standard	Requirement	How ORDR Delivers
§ 164.312(a)(1) — Access Control	Unique user identification and emergency access procedures for ePHI systems	Device-level access monitoring with anomaly detection on clinical systems adjacent to ePHI
§ 164.312(b) — Audit Controls	Hardware, software, and procedural mechanisms to record access to ePHI	Continuous behavioral logging for all connected clinical devices with exportable audit evidence
§ 164.312(c)(1) — Integrity	Protect ePHI from improper alteration or destruction	Behavioral baselines detect unauthorized access or modification attempts on clinical systems
§ 164.312(e)(1) — Transmission Security	Guard against unauthorized access to ePHI in transit	Network segmentation and encrypted communication enforcement for IoMT and clinical systems

FDA Cybersecurity Guidance

FDA Guidance	Requirement	How ORDR Delivers
Premarket Cybersecurity Guidance	SBOM documentation, vulnerability management plan, and security architecture evidence	SBOM-aware device inventory with CVE matching and continuous vulnerability monitoring
Postmarket Management	Coordinated vulnerability disclosure and continuous monitoring of deployed devices	Real-time device behavioral monitoring with automated alerting on anomalous activity
Security Patch Management	Process for identifying, testing, and deploying security updates to medical devices	Patch status tracking across all connected devices with risk-prioritized remediation workflows

Measured Results

Results That Protect Patients and Operations

Healthcare security is measured in patient safety maintained, care delivery protected, and compliance sustained.

Achieve complete IoMT visibility in days — passive deployment discovers every connected clinical device without touching them or disrupting care

Reduce device-related risk exposure by isolating high-risk assets — behavioral segmentation limits lateral movement without interrupting clinical workflows

Accelerate HIPAA compliance — continuous control monitoring with audit-ready evidence eliminates last-minute scrambles before assessments

Improve device utilization and uptime — accurate inventory data helps biomedical and IT teams manage device lifecycle and maintenance proactively

Respond faster to incidents — behavioral detection and automated containment reduce mean time to respond for clinical device-related security events

Medical Device Security FAQ