FDA Finalizes Medical Device Cybersecurity Premarket Guidance
The FDA has finalized guidance to assist medical device sponsors in addressing cybersecurity considerations as part of the premarket review process.
HTM’s Headlines
Editor's Picks
Fixing the Gap in Dental Equipment Repair
A new accredited program is addressing the lack of formal training in dental equipment repair and bringing the field closer to HTM.
Critical Resources
Protecting Patient Data
VA Report Flags Ongoing Sterile Processing Failures at Georgia Facility
A March 2025 report details ongoing VA sterile processing failures at the Carl Vinson VA Medical Center, including the use of damaged surgical instruments.
Staffing Essentials
Facility Fundamentals
Device Management 101
GE HealthCare Recalls Certain Carestation Devices Over Ventilation Risk
The Carestation anesthesia systems are being recalled due to a risk of ineffective ventilation in volume control mode, which could lead to serious injury or death.