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BioWorld - Monday, June 16, 2025

IDE

Home » Topics » Regulatory » IDE
  • Dbs for stroke 6 25
    Feb. 11, 2025
    By Shani Alexander

    Newronika gets IDE from the FDA for adaptive DBS trial

    Newronika SpA's AlphaDBS recently secured an investigational device exemption from the U.S. FDA allowing it to begin a pivotal trial to evaluate the safety and efficacy of its adaptive deep brain stimulation system in patients with movement disorders, including Parkinson's disease.
  • Deepqure 11june24
    June 11, 2024
    By Marian (YoonJee) Chu

    Deepqure gets FDA IDE nod for renal denervation device trial

    As renal denervation (RDN) makes a comeback for treatment-resistant hypertension, Deepqure Inc. is advancing its RDN medical device dubbed Hyperqure with the U.S. FDA granting clearance for a U.S.-based study.
  • Man mri prostate
    Aug. 9, 2022
    By Annette Boyle

    FDA advances AI-enhanced tech for prostate diagnosis and treatment

    Recent U.S. FDA actions could transform decades of prostate cancer care. Two companies focused on prostate cancer received good news from the FDA for their artificial intelligence (AI)-driven software. Bot Image Inc. gained FDA clearance for its medical device computer-aided detection and diagnostic tool, Prostatid. The agency also provided FDA investigational device exemption for Avenda Health Inc.’s Focalpoint ablation system that enables more accurate mapping of a patient’s prostate cancer for better surgical results.
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Authors

  • Meg Bryant
  • Liz Hollis
  • Annette Boyle
  • Mark McCarty
  • Catherine Longworth
  • Marian (YoonJee) Chu
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