AMED Ventures’ 2026 Annual LP Meeting Concludes Successfully
AMED Ventures held its 2026 Annual LP Meeting in Taipei on Thursday, September 10.
AMED Ventures held its 2026 Annual LP Meeting in Taipei on Thursday, September 10.
On September 10, 2026, AMED Ventures hosted its Annual International Medical Forum under the theme “Redefining Healthcare: A New Generation of Clinical Therapy Driven by AI, Robotics, and Medical Imaging.” The event welcomed more than 100 guests from the healthcare, technology, and investment communities.
AMED Ventures will convene an international medical forum in Taipei exploring how AI, robotics, medical imaging, and clinical needs are shaping the next generation of healthcare innovation.
Rejoni announced FDA premarket approval for its Juveena® Hydrogel System. The device is approved for adult women undergoing hysteroscopic surgery to treat symptomatic moderate to severe intrauterine adhesions, helping reduce both the occurrence and severity of postoperative adhesions.
Rejoni announced the closing of a $25 million financing to advance the Juveena Hydrogel System toward FDA approval and launch.
Tulavi Therapeutics' new hydrogel platform is bringing hope to trauma and amputation patients at risk of developing symptomatic neuromas.
Benthic Genomics announced the launch of Mako, a short-read immunogenomics analysis module on the Benthic Analysis Platform.
Supira Medical received FDA approval to initiate a new trial of its percutaneous ventricular assist device.
Imperative Care announced the enrollment of the first patient in the CLEAR-IT clinical study.
Kandu announced positive outcomes from a randomized controlled trial of the FDA-cleared IpsiHand brain-computer interface system.
Instylla announced the first commercial use of its Embrace Hydrogel Embolic System for peripheral vascular embolization.
Rejoni announced that the FDA filed its premarket approval application for the Juveena Hydrogel System.
Tulavi Therapeutics announced that its allay Hydrogel Cap received an Innovative Technology contract from Vizient.
Benthic Genomics announced the commercial launch of Angler Imputation on its cloud-based analysis platform.
Adona Medical completed enrollment in the ATHENS-HF first-in-human study of its interatrial shunt.
Atia Vision received FDA approval to begin a U.S. clinical trial of its OmniVu Lens System in patients with cataracts.
Kandu Health and Neurolutions merged to form Kandu Inc. and establish a new standard of care for stroke recovery.
Ostial Corp. acquired the Wavella technology from Crossfire Medical and unveiled its new identity as Verge Medical.
Instylla completed its premarket approval application submission for the Embrace Hydrogel Embolic System.
Rejoni completed patient enrollment in its pivotal clinical study of the Juveena Hydrogel System.
Tioga Cardiovascular announced the first-in-human implants of its Luna transcatheter mitral valve replacement system.
Adona Medical secured $33.5 million in Series C financing to advance solutions for heart failure.
The financing will support clinical trials, additional indications and expanded manufacturing capabilities for Akura Medical's thrombectomy platform.
Sealonix closed a $20 million Series A financing led by Excelestar Ventures.
康聚醫學科技是全臺唯一、全球少數的醫療用金屬線材供應商,承襲廣泰金屬集團四十多年的金屬加工技術。
康聚醫學科技憑藉專業抽線與自主修模技術,跨足醫療線材產業並開發心導管微創手術醫材。
Early ATHENS-HF trial data showed promise for an adjustable interatrial shunt in patients with heart failure.
Akura Medical began a pivotal trial of the Katana thrombectomy system in patients with pulmonary embolism.
Akura Medical secured financing to advance its thrombectomy system and clot-quantification software.
Imperative Care launched Ikon 24 as the latest addition to its comprehensive stroke-care portfolio.
Imperative Care raised $100 million to support its portfolio of technologies for stroke and vascular care.
Novo Holdings co-led a $120 million Series E financing to advance Supira Medical's percutaneous ventricular assist device technology.
The presentation reports initial outcomes for the Luna Mitral Valve Replacement System in patients with symptomatic mitral regurgitation.
Tulavi Therapeutics received FDA clearance for an absorbable hydrogel cap designed to protect the end of a severed nerve.
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