The Weekly Recap 2/7/25: LSI Alumni Achievements Driving Medtech and Healthtech Forward

In a successful week for the medical technology companies in the LSI Alumni community, we saw LSI Alumni launch new products, secure regulatory approvals, appoint new executives, and much more on the road to LSI USA ’25 in Dana Point, CA (March 17–21).

Arsenal Medical

Completed enrollment of an initial cohort of ten patients in its EMBO-02 clinical study of NeoCast to treat chronic subdural hematoma (cSDH). Neocast is a solvent-free, non-adhesive liquid embolic agent designed for effective deep distal penetration.

Cagent Vascular

Announced the launch of its most recent product, Serranator SL-PRO PTA Serration Balloon Catheter. The Serranator SL-PRO is specifically designed for pedal interventions and challenging-to-cross tibial disease.

CereVasc

Shared the initial results of its pilot clinical study evaluating the eShunt System for elderly patients with normal pressure hydrocephalus (NPH). The data supports the system’s potential as a minimally invasive alternative to traditional shunt surgery.

Gyder Surgical

Received FDA 510(k) clearance for its GYDER Hip System. The system is the world’s first commercially available pin-less/non-invasive, imageless solution for accurately positioning the acetabular cup during anterior hip arthroplasty.

Iantrek

Appointed LSI Alumni Adam Szaronos as Chief Executive Officer to lead the company’s next phase of growth. Szaronos, an ophthalmic industry executive, brings extensive experience in commercial strategy and medical device innovation.


This blog is originally published here: https://www.lifesciencemarketresearch.com/insights/the-weekly-recap-2725-lsi-alumni-achievements-driving-medtech-and-healthtech-forward 

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