No Carolina / NY / Florida
Ph: 561.316.3330

HomeMEDICAL DEVICES, TECHNOLOGIES, EQUIPMENT, SUPPLIES

Category: MEDICAL DEVICES, TECHNOLOGIES, EQUIPMENT, SUPPLIES

Adagio Medical Reports 1st ...

Adagio Medical, Inc. (“Adagio Medical”, “Adagio” or...

Richtech Robotics Launches Elevator Enabled...

With high operational accuracy, Medbot improves healthcare facility efficiency with a secure delivery, reducing operating costs and improving the overall patient experience. Medbot furthers Richtech Robotics’ mission of providing high-quality, stable robots to boost employee morale and improve customers’ bottom line.

Adagio Medical Reports 1st European Commercial Procedures and Commencement of U.S. FDA Pivotal IDE for Ventricular Tachycardia Cryoablation System

Adagio Medical, Inc. (“Adagio Medical”, “Adagio” or the “Company”), a leading innovator in catheter ablation technologies for ventricular tachycardia (“VT”) and atrial fibrillation (“AF”), today announced the completion of the first commercial procedures using its recently CE-Marked VT Cryoablation System and the U.S. Food and Drug Administration (“FDA”) approval of the FULCRUM-VT Pivotal IDE study of the VT Cryoablation System. VT procedures remain highly technical and time consuming, with a non-trivial rate of serious complications, and are predominantly performed in high-volume academic centers. The Adagio Medical VT Cryoablation System with...

PathKeeper Surgical Celebrates the First Spine Surgery Performed with the PathKeeper 3D Optical Navigation System in Massachusetts

The PathKeeper system was used at Southcoast Health's St. Luke's Hospital in New Bedford, MA, to improve the clinical experience, increase surgical accuracy and eliminate radiation exposure during surgery.

BD Advances “One-Stick Hospital Stay” Vision with Launch of Next-Generation Needle-Free Blood Draw Technology

With 510(k) clearance from the U.S. Food and Drug Administration (FDA), the new PIVO™ Pro Needle-free Blood Collection Device features design improvements to achieve the first and only compatibility with integrated and long peripheral IV catheters, including the new Nexiva™ Closed IV Catheter System with NearPort™ IV Access. This expands on current PIVO™ compatibility with traditional short peripheral IV catheters available since 2017.  

Ceribell Launches ClarityPro ™ AI, Expanding Access to Critical Diagnosis of Electrographic Status Epilepticus

ClarityPro is an AI-based software algorithm within the Ceribell EEG system that analyzes EEG waveforms to diagnose electrographic status epilepticus (ESE). It is the first acute care device to be FDA indicated for stand-alone diagnosis.

Medical Equipment Upgrades in the Dental Space: Revolutionizing Patient Care

In this article, we will explore the latest innovations in the dental space and delve into the importance of autoclaves in maintaining a safe and sterile environment.

Study Organized by Main Line Health Researchers Reverses FDA Warning on Vital Peripheral Artery Disease Treatment

Results of the study on devices coated with paclitaxel were presented today at the TCT 2023 meeting in San Francisco, the world’s largest interventional cardiology meeting. The study shows no increased risk of death from use of paclitaxel-coated devices and has simultaneously been published on a fast-track basis by The Lancet.

PeekMed Expands into the US with a New Subsidiary and New Product

The decision to form PeekMed LLC is driven by a desire to strengthen presence in the world's largest and most influential healthcare market. This expansion will enable PeekMed to offer versatile solutions and provide timely support to its growing customer base in the US.

ulrich medical USA® Announces Full U.S. Commercial Launch of the Momentum® MIS Posterior Spinal Fixation System

"Momentum MIS is truly among the leading next generation MIS solutions on the market in terms of performance and adaptability", said Jim Bruty, Chief Operating Officer at ulrich medical USA.Visit the ulrich medical booth (#1635) in Los Angeles to learn more.

Neoss ® Group Receives EU MDR Certifications for Implants and Abutments

"The MDR certification gives Neoss the freedom to continue innovating intelligent solutions that benefit our customer and their patients. The MDR certification also shows that Neoss products are backed with clinical evidence of the highest standard and ensures that the products are continuously monitored in post-market studies." Mr. Fredrik Engman, CTO and co-founder of Neoss."

Centinel Spine’s prodisc ® Continues to Change Lives After Over 30 Years and 250,000 Total Disc Replacement Implantations

The prodisc lumbar and cervical technologies will be highlighted by Centinel Spine at the upcoming 2023 annual EUROSPINE meeting and congress in Frankfurt, Germany (October 4-6, 2023). The prodisc technology portfolio now includes four cervical and two lumbar devices—5 approved by the FDA—and has been validated with a reported reoperation rate of less than 1%.

By using this website you agree to accept Medical Device News Magazine Privacy Policy