Reports Q1 revenue $3.4M, consensus $2.7M. “Our first quarter results reflect strong underlying demand and consistent clinical outcomes for our CGuard carotid stent implant both in the U.S. and internationally,” stated Marvin Slosman, Chief Executive Officer of InspireMD (NSPR). “While our decision to voluntarily pause commercialization of CGuard Prime 135 cm in the U.S. will impact its availability in the short term, we are in the process of implementing several enhancements to the delivery system that we are confident will elevate technical performance and accelerate rapid adoption. Importantly, our TCAR program is unaffected by this voluntary action, and we were also pleased to have recently received FDA approval to initiate the CGUARDIANS III clinical trial with our SwitchGuard NPS, which, if successful, would enable us to offer a full TCAR tool kit leveraging our best-in-class implant.”
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Read More on NSPR:
- InspireMD price target lowered to $4 from $5 at Lake Street
- InspireMD withdrawing prior FY26 revenue guidance
- InspireMD initiates voluntary U.S. recall of CGuard Prime 135 cm system
- InspireMD Recalls CGuard Prime Delivery System, Pauses U.S. Launch
- InspireMD announces FDA approval of IDE application for CGUARDIANS III study
