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InspireMD Announces Presentation of Positive One-Year

Data demonstrate lowest reported primary endpoint event rate of 1.95% through twelve months post-procedure for any carotid stent or embolic protection.

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Inspiremd Dips On Q1 Figures

Inspiremd Dips On Q1 Figures
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InspireMD Announces Abstract of One-Year Follow-Up Results from the C-GUARDIANS U S Investigational Device Exemption (IDE) Clinical Trial Accepted for Presentation at LINC 2024

TEL AVIV, Israel and MIAMI, March 26, 2024 InspireMD, Inc. , developer of the CGuard™ Embolic Prevention Stent System for the prevention of stroke, today announced that an abstract of the.

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InspireMD Announces Abstract of One-Year Follow-Up Results from the C-GUARDIANS U S Investigational Device Exemption (IDE) Clinical Trial Accepted for Presentation at LINC 2024

InspireMD Announces Abstract of One-Year Follow-Up Results from the C-GUARDIANS U S Investigational Device Exemption (IDE) Clinical Trial Accepted for Presentation at LINC 2024
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United statesMarvin slosmanChris metzgerChuck padalaClinical events committeeOhio healthExchange commissionCompany annual report on formInspiremd incOne year follow up resultsDevice exemptionClinical trial acceptedEmbolic prevention stent systemPrime carotid stent systemLeipzig interventional courseYear follow up results

InspireMD Presents Positive 30-Day Follow-Up Results from the C-GUARDIANS U S Investigational Device Exemption (IDE) Clinical Trial at VIVA23

InspireMD Presents Positive 30-Day Follow-Up Results from the C-GUARDIANS U S Investigational Device Exemption (IDE) Clinical Trial at VIVA23
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