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InterValve developed the V8 and TAV8 aortic valvuloplasty balloon catheters, which feature an anatomically shaped "8" design to optimize safety and efficacy during transcatheter aortic valve replacement (TAVR) procedures. These products received FDA approval and CE mark in 2013, with stable sales in the US and Europe prior to acquisition by Venus Medtech. Clinical use has shown improved outcomes such as reduced risk of annulus tearing and perivalvular leakage compared to traditional cylindrical balloons.
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