Vascular Dynamics Completes $20 Million Equity Financing to Support Further Clinical Evaluations of MobiusHD Device

Vascular Dynamics, Inc. (VDI), a privately held medical device company focused on developing game-changing endovascular device-based solutions for patients suffering from heart failure, has announced the closing of its $20 million financing round led by an investment partner of VDI shareholder Rainbow Medical. Lawrence C. Best also joined existing investors HBM Healthcare Investments and Invus in this equity round.

The Vascular Dynamics MobiusHD device is designed to provide interventionalists with a minimally-invasive transcatheter approach to help treat patients suffering from continued heart failure problems despite pharmaceutical therapy. Heart failure currently affects at least 26 million people worldwide and is increasing in prevalence.

Heart failure is often associated with an autonomic nervous system imbalance. Baroreceptors are specialized nerve endings that respond to stretch and are located along the carotid arteries in the neck. These stretch receptors are essential to the body’s natural control and performance of the cardiovascular system. The MobiusHD device is an endovascular implant designed to reshape the carotid artery and amplify this natural baroreflex mechanism, signaling the brain to produce autonomic modulation for improved heart function.

The funding announcement also comes on the heels of a live endovascular procedure using the MobiusHD device performed by Horst Sievert, MD, Director of the CardioVascular Center in Frankfurt, Germany during the recent CSI Frankfurt 2022 Congress. This procedure represented the 30th patient enrolled in the ongoing clinical trial entitled, “A Feasibility Study Exploring the Effect of the MobiusHD Device in Patients with Heart Failure.”

“Initial 12-month clinical results have shown impressive efficacy and demonstrated that the MobiusHD device provides a safe option to treat heart failure patients,” said Dr. Sievert, referring to the study.

“We are excited to be moving into the next phase of our company’s evolution,” said Ed Roschak, CEO of Vascular Dynamics. “Patients who remain symptomatic despite medical therapy need another option. We believe our device-based treatment can provide a solution. This new round of funding will enable us to further expand the pilot study and sets the stage for a forthcoming pivotal study.”

“We are pleased to support the extended clinical evaluation of the MobiusHD device as a new potential therapeutic approach to treating this global patient population,” said investor and new Vascular Dynamics board member Lawrence C. Best. “We are proud to invest in VDI and this novel technology.”

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”