R3 Vascular Inc. Completes Series A Financing Round and New Chief Executive Officer

October 8, 2020

R3 Vascular today announced closing of its Series A financing round, including new equity investments of $15 million and the conversion of $2.8 million of convertible notes. The round was led by an unnamed corporate investor and 415 CAPITAL, with participation from HBM-MedFocus LLC and Wexford Capital.

R3 Vascular reports the proceeds will support the company’s clinical trial work in developing a next generation of below-the-knee (BTK) interventional therapies for PAD.

R3 Vascular Executive Chairman Jack Springer said, “We are excited about this investment in the company’s future. The number of patients suffering from BTK vascular disease is growing significantly for many reasons, including a large global increase in diabetes and obesity. These factors, along with others, are leading to a rapid rise in critical limb ischemia (CLI), a severe form of PAD. The physician community has been waiting far too long for a more safe and effective way to treat BTK disease.”

Springer added, “I am further pleased to announce that Kamal Ramzipoor will join R3 Vascular as CEO,” said Mr. Springer. “Kamal has extensive experience in building and leading both early-stage and large medical device companies. In particular, he is a hands-on leader with extensive experience in developing and commercializing polymer-based drug/device combination products.”

Mr. Ramzipoor added, “The unique mechanical properties and polymer technology of R3 Vascular’s proprietary bioresorbable scaffold, already validated in multiple clinical trials, offer differentiating features compared to other bioabsorbable scaffolds. It is becoming clear that the use of scaffold support offers a potential competitive advantage compared to other balloon-based therapeutic approaches in BTK interventions. R3 Vascular’s polymeric technology is the only platform that has achieved ‘DES-like’ mechanical performance at the sub-100-micron level across all scaffold diameters.”

Dr. Juan Granada, a key strategic advisor to R3 Vascular, stated that “A resorbable sirolimus-eluting device provides the best of both worlds for this type of patient: acute mechanical support, long-term lumen patency and progressive resorption allowing vessel re-intervention in case it is needed. The superior mechanical performance of the R3 Vascular bioresorbable platform has the potential to shift the therapeutic approach for patients suffering from CLI.”

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.”
Exit mobile version