Intuitap Medical Close Successful $5.5m Series A Round of Funding Led by the Pink Ceiling and Curate Capital

IntuiTap Medical, a cutting-edge medical device company with technology poised to change the spinal tap, announced today the closing of their Series A investment round.

The transaction was led by The Pink Ceiling, IntuiTap’s largest investor, and Curate Capital. This latest raise will be used to take IntuiTap’s novel VerTouch technology through final clinical trials at the University of Texas, the Medical University of South Carolina, and Rhode Island Hospital, and through a submission to the FDA for approval.

VerTouch eliminates the guesswork from spinal punctures, reducing physician frustration, patient pain, and costly trips to radiology. The current standard of care for spinal punctures requires physicians to feel patients’ vertebrae and blindly insert a needle. This method results in first attempt failures in as high as 60% of cases, requiring multiple insertions to properly place the needle.

IntuiTap’s first in class technology eliminates that guesswork by providing physicians 2D imaging of the patient’s vertebrae and needle guidance all in the palm of their hand. The device has demonstrated a 90+% single-insertion success rate, and can be used at the patient’s bedside, significantly reducing the need for costly radiological intervention.

“IntuitTap and Jessica Traver-Ingram just changed the game for women’s healthcare. The need to perform multiple dreaded spinal punctures due to high failure rates is now virtually eliminated thanks to an innovative new device. Patients get to breathe a big sigh of relief while the medical industry saves considerable time and money. That’s a big win for everyone”, said Cindy Eckert, CEO of The Pink Ceiling and IntuiTap Investor.

“At Curate Capital, we invest in businesses built by women for women,” said Carrie Colbert, Founding Partner of Curate Capital and IntuiTap investor. “We love that IntuiTap is solving a literal pain point for millions of women! Beyond that, we invest in winning women – and that’s exactly who Jessica Traver-Ingram is.”

“IntuiTap is entering our exciting final step toward FDA approval. With the current capital raise and the strength of the caliber of investors we have in the company, we feel very optimistic about the lasting change we can make on the healthcare system,” said Jessica Traver-Ingram, IntuiTap CEO, “Our device is going to save doctors’ and patients’ time, and reduce frustration, pain, and complications for one of the most common procedures in the hospital setting.”

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