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Medical Device Startup Exceeds $40M Series B Funding Goal

Key Points
  • Jupiter Endovascular raised over $40 million in an oversubscribed Series B round led by Sonder Capital, with Senvest Management, LB Investment, and a strategic corporate investor participating.
  • The funds will support completion of the SPIRARE II pivotal trial, prepare the company for commercialization, and expand applications of its Transforming Fixation technology platform.
  • Jupiter's Vertex Catheter received FDA 510(k) clearance last month, while first-in-human trial results will be presented at TCT 2025 in late October.
October 7, 2025
Sonder Capital Leads Jupiter's Oversubscribed Series B Round
Credits: Jupiter official website

Jupiter Endovascular has closed an oversubscribed Series B financing round that exceeded its $40 million target. The round was led by Sonder Capital, with participation from Senvest Management, LB Investment, and a new strategic corporate investor. The medical technology startup is developing a new class of endovascular procedures using its proprietary Transforming Fixation (TFX) technology.

The company plans to use the proceeds to complete its ongoing SPIRARE II pivotal clinical trial, prepare for commercialization, and develop new clinical applications for the TFX platform. The funding arrives at a significant moment for Jupiter: the company received FDA 510(k) clearance for its Vertex™ Catheter incorporating TFX last month, and will present first-in-human results from the SPIRARE I trial later this month at the Transcatheter Cardiovascular Therapeutics Conference (TCT 2025) in San Francisco.

Addressing a Major Challenge in Cardiovascular Intervention

The TFX platform addresses what many consider one of the most significant challenges in transcatheter interventions: maintaining stability and control while operating in complex cardiovascular anatomies. Jupiter is initially focusing on pulmonary embolism, a condition that affects hundreds of thousands of patients annually.

"Closing this oversubscribed Series B financing round reflects strong conviction in our mission to rewrite the rules of endovascular medicine using TFX technology," said Carl J. St. Bernard, CEO of Jupiter Endovascular. "We're energized by the support of this distinguished syndicate of investors as we tackle one of the greatest unmet needs in transcatheter interventions - the lack of stability and control physicians face while operating in complex cardiovascular anatomies - starting with pulmonary embolism."

Clinical Trial Progress and Commercial Preparations

The funds will primarily support the SPIRARE II trial (NCT06576427), a prospective, single-arm, multicenter pivotal study. The trial will enroll up to 145 patients with acute, intermediate-risk pulmonary embolism treated with the Vertex Pulmonary Embolectomy System at up to 25 sites in the U.S. and Europe. Endpoints will measure safety, right heart function, and clinical improvement from the procedure through 30 days post-procedure.

Results from the earlier SPIRARE I study (NCT06571760) will be presented on October 26 at TCT 2025. That study enrolled 10 subjects with acute, intermediate-risk PE at two European sites. Professor Irene Lang, Principal Investigator and Professor of Vascular Biology at the Medical University of Vienna, will present the findings.

How the Technology Works

The Vertex system uses Jupiter's TFX platform to provide stability during catheter-based procedures. The device is delivered in a flexible, relaxed state over a guidewire to a target location in the vasculature. It's then rapidly pressurized with saline to fix it in a stable position for intervention. After the procedure, it returns to its relaxed state to navigate to another location or for removal.

This approach is designed to enable interventionalists to treat anatomical sites that are not safely or easily accessible via conventional endovascular approaches. The technology aims to provide stability even in tortuous anatomies while protecting the cardiovascular anatomy.

Company Background and Mission

Jupiter Endovascular is focused on expanding the boundaries of endovascular medicine through its TFX platform technology. The company was founded to address the longstanding challenge of maintaining catheter control during procedures, which has limited the adoption of transcatheter therapies in certain complex cases.

The startup is initially targeting pulmonary embolism but plans to expand into additional high-need cardiovascular applications. By allowing interventionalists to navigate flexibly through the vasculature and then stabilize with control at the treatment site while remaining conformed to the anatomy, Jupiter aims to make catheter-based therapies accessible to more patients.

Investor Perspective and Historical Funding

"Since the earliest days of endovascular medicine, the inability to maintain catheter control has been the single greatest barrier to the wider adoption of transcatheter therapies," said Deborah Kilpatrick, PhD, Partner at Sonder Capital. "Jupiter is addressing this vast unmet need with a revolutionary advance that can provide stability in even the most tortuous anatomies, unlocking new possibilities for the millions of patients who are being underserved with today's intravascular approaches. We are proud to lead this round and to partner with Carl and the Jupiter team to bring this technological breakthrough to physicians and patients worldwide."

Sonder Capital's team includes veteran investors, innovators, founder-operators, and company builders. The firm was co-founded in 2019 by healthcare luminaries Jay Watkins and Fred Moll, M.D. The firm's portfolio and network includes involvement with companies like Intuitive Surgical (NASDAQ:ISRG), Procept Biorobotics (NASDAQ:PRCT), Shockwave Medical, Auris Health, and Reflexion Medical.

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