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AngioScore developed and commercialized the AngioSculpt Scoring Balloon Catheter for both coronary and peripheral interventional markets. The uncoated version was FDA-cleared and commercially available. A drug-coated version entered First-in-Human clinical studies targeting coronary in-stent restenosis with endpoints including late lumen loss and major adverse cardiovascular events. Preclinical data showed safety and efficacy in reducing restenosis rates; clinical results were pending as of last public updates.
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