New Federal Guide Outlines Zero Trust Strategies for Operational Technology
The joint report addresses cybersecurity challenges for legacy infrastructure and physical safety requirements in facility and industrial systems.
Category: Standards
Standards
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Standards
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MITRE Report Outlines Cybersecurity Risks for Medical Devices Using AI and Cloud
The analysis identifies emerging threats to patient safety and device performance as manufacturers adopt new technologies and advanced encryption.
Standards
Latest
Social Engineering Drives 88% of Healthcare Cybersecurity Losses
A new report finds that average cyber insurance claim severity in the healthcare sector exceeded $2 million per incident in 2025.
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Texas Directs Healthcare Facilities to Align With FDA Medical Device Cybersecurity Guidance
State officials are urging hospitals to review device cybersecurity risks and align policies with FDA guidance.
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FDA Clears Deep Learning Technology for High-Resolution CT Imaging
The software is designed to enhance spatial resolution and suppress artifacts in pulmonary, musculoskeletal, and inner ear scans.
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Restore Robotics Receives FDA Clearance for Additional Remanufactured da Vinci Xi Instruments
Clearances expand options for hospitals seeking lower-cost alternatives to OEM robotic surgical instruments.
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FDA Clears Medtronic Surgical System for Cranial and ENT Procedures
The platform combines planning, navigation, and robotics, with AI-enabled features for imaging and workflow support.
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Boston Scientific Receives FDA Clearance for Asurys Fluid Management System
Device is designed to regulate irrigation and intrarenal pressure during endoscopic urologic procedures
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Philips Receives FDA Clearance for AI Software to Guide Mitral Valve Repair
EchoNavigator with DeviceGuide uses AI to track and visualize repair devices in real time during minimally invasive procedures.
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MARS Bioimaging Gains FDA Clearance for Portable Photon-Counting CT Scanner
The extremity-focused system is designed for point-of-care use, including clinics and ambulatory settings.
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Could Vermont Crack the Code on Right to Repair? (Editor’s Message)
A recent hearing in Vermont shows lawmakers are asking more pointed questions about medical device repair. What happens next may depend on whether HTM professionals speak up.
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GE HealthCare’s Photonova Spectra Photon-counting CT Receives FDA Clearance
The cleared system introduces photon-counting CT designed to capture spectral data in a single scan and reduce protocol complexity.
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Defibrillation Lead Wins FDA Approval for Conduction System Pacing
The defibrillation lead, approved for placement in the left bundle branch area, can deliver both life-saving shock therapy and physiologic pacing through the heart’s natural electrical system.
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CISA Issues Alert on Endpoint Management System Security After Stryker Cyberattack
Federal agency calls on healthcare and medical technology organizations to tighten endpoint management controls following attack on Stryker’s Microsoft environment.
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