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Urban Fire Forum with NFPA Endorses Position Paper Advocating the Use of Neuroprotective Head Up CPR as Standard of Care for First-In Responders

Fire chiefs from Canada, Mexico, the United Kingdom, and the U.S. participated in the National Fire Protection Association® (NFPA®) Urban Fire Forum (UFF) last week at NFPA headquarters in Quincy, MA, endorsing five important…

The FDA Approves IDE for ReGelTec’s Pivotal Study HYDRAFIL for Chronic Low Back Pain due to Degenerative Disc Disease

ReGelTec, Inc., announced that the U.S. Food and Drug Administration has approved an IDE for the company’s pivotal study to support premarket approval of its HYDRAFIL® System. The HYDRAFIL System…

Regenesis Achieves FDA Clearance for the New Reprieve by Regenesis Device

Regenesis Biomedical, Inc., a medical devic­­e company focused on safe, non-drug, pain management, announced today commercialization of the new Reprieve by Regenesis™ device (Reprieve).  Reprieve is the only home-use shortwave…

Francis Medical Announces First Patient Treated in VAPOR 2 Pivotal Study for Water Vapor Ablation of Prostate Cancer

Francis Medical, Inc., a privately held medical device company developing an innovative and proprietary water vapor ablation therapy for the treatment of prostate, kidney, and bladder cancer, today announced the…

OBVIUS Robotics™ Announces Completion of Successful First-In-Human Cases

Obvius Robotics, Inc., a medical device company that has developed an innovative technology platform for performing percutaneous access, today announced the successful completion of its first human cases.

Tempus Receives U.S. FDA Approval for xT CDx, a NGS-Based In Vitro Diagnostic Device

Tempus, a leader in artificial intelligence and precision medicine, today announced that the U.S. Food and Drug Administration (FDA) has approved the company’s first Premarket Approval (PMA) application for its…

Clinical Study Results of the BlueWind System for Patients with Overactive Bladder Featured at the 2023 AUA Annual Meeting

 BlueWind Medical, Ltd., the developer of a transformative implantable tibial neuromodulation therapy for Overactive Bladder (OAB), today announced results from the OASIS pivotal trial evaluating the safety and efficacy of…

stethoscope

Terumo Blood and Cell Technologies’ IMUGARD Platelet Pooling Set Cleared by FDA

RefleXion Medical, a therapeutic oncology company, today announced the U.S. Food and Drug Administration (FDA) has granted the first marketing clearance for its SCINTIX™ biology-guided radiotherapy, a cutting-edge treatment applicable…

RefleXion Receives FDA Clearance for SCINTIX Biology-Guided Radiotherapy

RefleXion Medical, a therapeutic oncology company, today announced the U.S. Food and Drug Administration (FDA) has granted the first marketing clearance for its SCINTIX™ biology-guided radiotherapy, a cutting-edge treatment applicable…

UroMems Initiates First-in-Human Study of Its Smart Implant to Treat Stress Urinary Incontinence

UroMems announced today that it has successfully completed the first-in-human implant of the UroActive™ System, the first smart automated artificial urinary sphincter (AUS) investigational device to treat SUI.

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