Medical Technologies

Medical devices, digital health, medical artificial intelligence, surgical robots, and diagnostic technologies.

107 Articles

Government Report: Cybersecurity, Data Integration, and Skills Shortages Hinder the Digitization of Healthcare in Egypt

Medical Technologies

Government Report: Cybersecurity, Data Integration, and Skills Shortages Hinder the Digitization of Healthcare in Egypt

A report issued by the Information and Decision Support Center of the Cabinet reviews the growth of the global digital health market and Egypt’s efforts to digitize its healthcare services, including the creation of 4.5 million electronic health records and the issuance of more than 42 million electronic prescriptions. The report warns that accelerating the transformation requires addressing data security, interoperability, and the shortage of specialized expertise.

2026-08-31

U.S. Court Orders Guardant Health to Pay More Than $245 Million in Patent Dispute

Medical Technologies

U.S. Court Orders Guardant Health to Pay More Than $245 Million in Patent Dispute

A U.S. court issued a final judgment requiring Guardant Health to pay more than $245.2 million to TwinStrand Biosciences and the University of Washington after finding it had willfully infringed two patents covering DNA sequencing technologies. The judgment also includes 6% royalties on sales of 11 products and a service until the patents expire in March 2033, while the company plans to appeal the decision.

2026-08-26

FDA Requests Public Comment on Classifying Certain Medical Device Accessories as Class I Devices

Medical Technologies

FDA Requests Public Comment on Classifying Certain Medical Device Accessories as Class I Devices

The FDA’s Center for Devices and Radiological Health has issued a proposed list of medical device accessories that may be eligible for independent classification as Class I devices and opened a comment period through October 16, 2026. The action does not mean that the classification has already been approved; rather, it aims to identify accessories for which general controls are sufficient to provide reasonable assurance of safety and effectiveness.

2026-08-25

FDA Selects First Participants in READI-Home Challenge to Develop Devices That Reduce Hospital Readmissions

Medical Technologies

FDA Selects First Participants in READI-Home Challenge to Develop Devices That Reduce Hospital Readmissions

The U.S. Food and Drug Administration has selected initial participants to advance to the interaction phase of the READI-Home Challenge, which aims to accelerate the development of medical devices for home use after hospital discharge. The current list includes a system for monitoring electrical brain activity and a therapeutic vibrating mattress for infants, while applications continue to be accepted through September 30, 2026.

2026-08-24

Turkcell Performs Remote Robotic Surgery via 5G and Network Slicing Technology

Medical Technologies

Turkcell Performs Remote Robotic Surgery via 5G and Network Slicing Technology

Turkcell conducted a remote robotic surgery demonstration between the Turkish ship TCG Anadolu and Kocaeli University, using a 5G network and network slicing technology to isolate data traffic and provide a secure, real-time connection. The company says the demonstration made the ship the first military naval vessel of its kind among Mediterranean countries to have a robotic surgery infrastructure.

2026-08-22

FDA Authorizes Claria System for Tissue Containment During Laparoscopic Uterine Surgery and Reaffirms Risks of Uncontained Morcellation

Medical Technologies

FDA Authorizes Claria System for Tissue Containment During Laparoscopic Uterine Surgery and Reaffirms Risks of Uncontained Morcellation

The U.S. Food and Drug Administration authorized the Claria System for marketing, a device that combines tissue morcellation and containment during certain laparoscopic uterine surgeries. The agency emphasizes that electromechanical morcellators should be used only in selected patients and with a compatible containment system because of the risk of spreading undetected uterine cancer.

2026-08-20

U.S. Food and Drug Administration Authorizes Vitestro’s Robotic Blood-Draw Device

Medical Technologies

U.S. Food and Drug Administration Authorizes Vitestro’s Robotic Blood-Draw Device

The U.S. Food and Drug Administration has authorized Vitestro’s Aletta, a robotic system that uses imaging, ultrasound, and artificial intelligence to draw blood samples without direct manual intervention by a specialist throughout the procedure. The device may allow one specialist to supervise up to three devices at a time, as the United States faces a shortage of workers trained in blood collection.

2026-08-20