Trusted byOracleSnowflakeCloudflareLinkedInGoogleSalesforce★★★★★4.8/5 on G2
LaunchCagent Vascular, Inc. launches the POINT FORCE Registry to evaluate the safety and efficacy of the Serranator® PTA Serration Balloon Catheter.
Jan 28, 2025
WayneHealthcareHealth Care
Product Description
Cagent Vascular has initiated the POINT FORCE Registry, a post-market clinical study to assess the safety and efficacy of the Serranator® PTA Serration Balloon Catheter for treating Peripheral Artery Disease. This multicenter study will enroll at least 500 subjects across the United States.
Company Information
Company
Cagent Vascular
Location
150 STRAFFORD AVENUE
Wayne, Pennsylvania, United States
About
Cagent Vascular has developed and commercialized its novel angioplasty balloon with Serration Technology to treat blocked arteries in the leg or Peripheral Artery Disease (PAD) and Chronic Limb Threatening Ischemia (CLTI). The Serranator PTA Serration Balloon Catheter is the first and only angioplasty balloon with serration technology.
AI made execution free. Knowing first is the whole game now.
Fundz sees it the moment Cagent Vascular ships something new, hires an exec or expands, usually minutes after it happens, and tells you who to reach.