Angioscore, Inc.

Contact: Michael Gioffredi - VP Marketing & Sales
Address: 5055 Brandin Court, Fremont, California 94538, USA
Phone: +1-(510)-933-7900, 877-264-4692 | Fax: +1-(510)-933-7901 | Map/Directions >>

Profile: Angioscore, Inc. offers balloon catheters for treating both peripheral arterial disease (PAD) and coronary artery disease (CAD). The innovative nitinol scoring element in our products scores the plaque circumferentially, providing a precise and predictable dilatation across a wide range of lesion types. Our AngioSculpt® PTA Scoring Balloon Catheter significantly alters the landscape for treating PAD. This catheter has been proven effective in complex calcified lesions (67.4%), bifurcation (25.6%), and ostial (15.1%) lesions. It has a record of significantly low dissection rate and successful deployment in 98.8% of lesions. Semi-compliant balloon material allows the physician to tailor the device size to the vessel (2-20 atm) depending on the size of the balloon. Nitinol-enhanced balloon deflation offers excellent rewrap and recross capabilities. AngioSculpt® PTCA Scoring Balloon Catheter is used for treating CAD. It treats complex lesions, including in-stent restenosis (ISR) and type C lesions. It offers freedom from major adverse cardiac events. This is the only coronary balloon catheter with specific indication for treating type C lesions.

The company was founded in 2003 and is CE certified.

FDA Registration Number: 3005462046

5 Products/Services (Click for related suppliers)  
• Angiographic Balloon Catheter
• Balloon Catheters
• Cutting/Scoring Percutaneous Transluminal Coronary Angioplasty (Ptca) Catheter (FDA Code: NWX)
• Percutaneous Catheter (FDA Code: DQY / 870.1250)
A percutaneous catheter is a device that is introduced into a vein or artery through the skin using a dilator and a sheath (introducer) or guide wire.
• Peripheral Transluminal Angioplasty Catheter (FDA Code: LIT / 870.1250)

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