Healthcare Cybersecurity
A

Armis

Cyber exposure management platform covering the full cyber-physical systems landscape, with medical device security as one of five products within Armis Centrix alongside Asset Management, OT/IoT Security, ViPR Pro for vulnerability prioritisation and remediation, and Early Warning. The platform correlates device context, behavioural anomalies, vulnerability intelligence, business impact and exposure pathways into a unified risk model, prioritising remediation by real-world operational risk rather than treating findings in isolation. Named a Leader in the 2026 Gartner Magic Quadrant for CPS Protection Platforms for the second consecutive year, one of 13 vendors evaluated, and recognised in the companion Critical Capabilities report, with 119 Gartner Peer Insights reviews in that category rating 4.7 out of 5 as of March 2026. Offers on-premise, cloud and hybrid deployment. TWO THINGS A READER MUST WEIGH, both stated plainly by the company. First, this is a HORIZONTAL platform, not a healthcare specialist: it serves manufacturing, energy, critical infrastructure and government alongside healthcare, and medical device security is one product line rather than the business. It is indexed on the same basis as Claroty, whose Medigate-derived healthcare capability sits inside a broader industrial security platform. Buyers should compare it against healthcare-only vendors such as Cylera and Asimily on depth of clinical device intelligence rather than on platform breadth, and independent Gartner Peer Insights commentary notes that while asset visibility is strong, some users find OT and CPS protocol depth less than top tier. Second, INDEPENDENCE IS ENDING: Armis has announced a planned acquisition by ServiceNow expected to complete in the second half of 2026. The company states it will continue operating with the same mission and innovation strategy under ServiceNow investment. That should be treated as a forward-looking statement rather than a settled outcome, and buyers signing multi-year agreements should establish what contractual continuity exists. The pattern is worth watching: an independent exposure management platform absorbed by an enterprise workflow vendor raises the same question as diagnostics manufacturers acquiring open algorithm platforms.

Last VerifiedJuly 21, 2026
Compare Armis with other vendors
Founded
Headquarters
San Francisco, California, United States
Website
www.armis.com
Categories
healthcare-cybersecurity, healthcare-admin-automation
Assessment

Capability Axes

AI Capability
AI Centrality
B
Third Party Estimated

Deliberate B, applying the same reasoning used for Nanox.AI, graded down because it is one line of a larger business. The analytical work is real: Armis Centrix correlates device context, behavioural anomalies, vulnerability intelligence, business impact and exposure pathways into a unified risk model, and behavioural anomaly detection across an asset estate of this breadth is genuinely model-driven. But medical device security is one of five products on a horizontal platform whose centre of gravity is cyber-physical systems across manufacturing, energy and critical infrastructure, and the platform's core asset is the breadth of its device intelligence across all those domains. Compare Ordr and Cylera, both graded A, where the ML is the whole product and healthcare is the whole market.

Autonomy and Oversight Model
B
Third Party Estimated

Risk prioritisation and remediation guidance integrated into enterprise workflows rather than autonomous enforcement, with the ViPR Pro product specifically handling vulnerability prioritisation and remediation. The stated design intent is addressing critical exposures quickly while minimising operational disruption, which is the correct framing for environments where enforcement error is consequential. Graded B rather than A because no explicit human approval gate or enforcement simulation capability was described in located materials, unlike Ordr which documents simulating enforcement impact and showing blast radius before rules change.

Model and Technology Transparency
C
Third Party Estimated

Product architecture is clearly enumerated at the five-product level and the risk model inputs are named, covering device context, behavioural anomalies, vulnerability intelligence, business impact and exposure pathways. But no detection methodology, training data description, model detail or accuracy figures were located, and the language is consistently platform-level rather than technical. The index's category editorial requires named detection methodologies rather than marketing language, and Armis sits below that bar relative to Cylera, which explains its Digital Twin mechanism, and Bluesight, which names unsupervised learning explicitly.

Clinical and Operational Evidence
B
Third Party Estimated

The strongest analyst validation in this category, though not healthcare-specific. Named a Leader in the 2026 Gartner Magic Quadrant for CPS Protection Platforms for the second consecutive year among 13 evaluated vendors, and recognised in the companion Critical Capabilities report which scores product functionality across four use cases. Gartner Peer Insights carries 119 reviews in the CPS category at 4.7 out of 5 as of March 2026, with 267 ratings across all markets, which is substantial independent customer feedback. Graded B rather than A for two reasons: the recognition is for CPS protection broadly rather than medical device security specifically, so it does not establish healthcare depth, and peer reviews include a substantive criticism that OT and CPS protocol understanding is basic rather than top tier with limited ability to alert on true OT-specific threats. No healthcare outcome data or KLAS healthcare ranking was located, unlike Asimily and Ordr.

AI Safety and PHI Stewardship
Not rated

No published detail located on data handling, retention or PHI treatment in clinical deployments. The on-premise deployment option materially reduces exposure for organisations that select it, since data need not leave the environment, but no specific policy statement was retrieved.

Regulatory and Compliance
HIPAA and BAA Posture
Not rated

No published BAA terms or HIPAA posture statement located at the time of review.

Security Certifications and Trust Center
Not rated

No specific third party attestation was retrieved at the time of review, consistent with every other vendor in this category. Note that a Gartner Magic Quadrant Leader placement is analyst recognition of market position and capability, not a security attestation, and the two should not be conflated.

FDA and Regulatory Status
Not rated

Not an FDA regulated product; the platform secures medical devices rather than performing a medical function. Same position as every device security vendor in this category.

AI Governance and Bias Disclosure
Not rated

No governance framework or model evaluation disclosure located. The relevant risk class is device classification coverage rather than demographic bias: on a platform spanning IT, OT, IoT, IoMT, cloud and code, uneven model performance across asset classes would leave specific device populations under-protected, and the peer review criticism regarding OT protocol depth suggests coverage is genuinely uneven across domains. No published analysis of classification accuracy by asset class was located.

Integration and Deployment
EHR and Interoperability Depth
A
Third Party Estimated

Integration into enterprise security workflows is the platform's stated design principle, replacing fragmented point solutions with a single contextualised view spanning IT, OT, IoT, IoMT, cloud and code, and peer reviewers specifically credit smooth integration with existing security tooling and a multitude of available data sources. Breadth of asset class coverage in one platform is the differentiator against healthcare-only competitors. The pending ServiceNow acquisition is directly relevant to this axis, since deep integration with the dominant enterprise ITSM and workflow platform would be a substantial interoperability advantage if realised, and buyers should factor that into a multi-year view.

Deployment Model and Data Residency
A
Vendor Published

The most flexible deployment position in this category. Armis offers on-premise, cloud AND hybrid options, explicitly so organisations can align the platform with their own infrastructure strategy while retaining a consistent security model. That materially exceeds the cloud-only posture of Asimily, Ordr and Cylera, and gives healthcare organisations with data sovereignty or residency constraints a genuine choice, which otherwise only Circle CVI provides in a different category. No specific residency terms located, but the architectural options themselves resolve most of the concern.

Commercial
Commercial Transparency
C
Third Party Estimated

No pricing published and no pricing basis disclosed. The five-product platform structure means a healthcare buyer needs to establish whether Medical Device Security can be licensed independently or requires broader platform adoption, and that is not public. Independent analysis in this category has noted that enterprise configuration costs for major platforms can be very high, so the variance is material and undisclosed.

Setting and Specialty Coverage
A
Third Party Estimated

The broadest coverage of any vendor in this category, spanning IT, OT, IoT, IoMT, cloud and code assets across healthcare, manufacturing, energy, critical infrastructure and government, delivered through five products covering asset management, OT and IoT security, medical device security, vulnerability prioritisation and early warning. For a health system that also operates industrial plant, building management systems and conventional IT, a single platform covering all of it is a genuine consolidation argument. The trade-off is the one this record flags throughout: breadth is bought at some cost in healthcare-specific depth relative to Cylera or Asimily.

Commercial

Pricing

Vendor-published figures are labeled as such. Figures labeled “Estimated” are derived from third-party sources and have not been confirmed by the vendor.

Entry Price Pricing Basis BAA Tier Implementation Source
Not published
Undisclosed. Five-product platform; confirm whether Medical Device Security licenses standalone. Pending ServiceNow acquisition H2 2026 may affect future packaging. Third Party Estimated

No pricing published and no pricing basis disclosed. The platform structure is the first thing a healthcare buyer must resolve: Armis Centrix comprises five products, Asset Management, OT/IoT Security, Medical Device Security, ViPR Pro and Early Warning, and whether Medical Device Security can be licensed standalone or requires broader platform adoption is not public. That determines whether Armis is competing on price against healthcare-only vendors such as Cylera and Asimily, or is a larger platform purchase justified by consolidating other security tooling. The consolidation case is the real commercial argument here, and it is legitimate: a health system that also runs building management systems, industrial plant and conventional IT may replace several point solutions with one platform, which changes the comparison entirely. Buyers should model total tooling displaced rather than comparing licence to licence. Deployment flexibility also has cost implications worth surfacing, since on-premise deployment shifts infrastructure cost to the customer while cloud does not, and Armis is unusual in this category in offering both plus hybrid. THE TIME-SENSITIVE POINT: Armis has announced a planned acquisition by ServiceNow expected to complete in the second half of 2026. Buyers negotiating now should seek explicit contractual continuity on pricing, product roadmap and support terms surviving the transaction, and should consider whether future packaging alongside ServiceNow licensing could change the economics. The company states it will continue operating with the same mission and innovation strategy, but that is a forward-looking statement rather than a contractual commitment.

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Index Status
Last index update
July 21, 2026
The AI Health Index is an editorial reference, not a regulatory body. Vendor data is verified against published sources and public regulatory filings. Figures labeled “Estimated” have not been confirmed by the vendor. See the Methodology page for evaluation standards and limitations.
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