Medical device company InspireMD, Inc. (NASDAQ:NSPR) announced on Friday that it has received CE Mark certification under the European Medical Device Regulation (MDR) for its CGuard Prime Embolic Prevention System (EPS), a carotid stent designed to prevent stroke.
The CGuard Prime incorporates user-driven enhancements to improve device deliverability and deployment, while maintaining the core design of the original CGuard system. Its proprietary MicroNet mesh technology is engineered to minimise embolic events by trapping arterial debris and preventing plaque prolapse and embolisation.
The approval paves the way for the commercial launch of CGuard Prime EPS within CE-marked markets, while aligning with InspireMD's strategy to expand into the United States, pending FDA approval later this year.
CGuard EPS is targeted at patients at high surgical risk, offering a less invasive solution with sustained embolic protection. Long-term results have demonstrated effectiveness beyond five years.
Saluda Medical secures CE certification for EVA Sensing Technology in Europe
Antin to acquire clinical trial equipment provider Emsere
Hyphens Pharma licenses Cerapro skin cream to Louis Widmer for six European markets
Profusa signs French distributor to expand Lumee Oxygen rollout in Europe
Sensiva Health names new chief operating officer
BrioHealth Solutions enrols 100th participant in BrioVAD System trial
Abbott's Amplatzer Piccolo Delivery System receives US FDA clearance and CE Mark
Amphix Bio announces initial closing of USD12.5m seed financing round
Bioretec wins FDA breakthrough status for biodegradable orthopaedic DrillPin
Amferia raises EUR3.5m to advance antimicrobial wound-care platform
BioCryst wins FDA approval for oral HAE prophylaxis in young children
ALR Technologies announces GluCurve Pet CGM relaunch in Canada
Galderma secures EU MDR certification for Sculptra, expanding use to multiple body areas
Clinical Laserthermia Systems applies for CE marking of ClearPoint Prism neuro laser system