Q’Apel Medical, Inc. Awarded U.S. Patent for Its Highly Innovative SelectFlex™ Technology

Q’Apel Medical, Inc., an innovative neurovascular company specializing in developing and commercializing novel access device technology for vascular interventions, is pleased to announce today that the United States Patent & Trademark Office has granted the company U.S. Patent No. 11,123,522 covering important features of its differentiated dual-mode catheter designs.

The SelectFlex™ variable stiffness technology provides unparalleled tracking and support in neurovascular access cases. Comprised of two operational modes, tracking mode and support mode allows physicians to switch between modes on-demand in a clinical case. By injecting 0.2cc of saline, and the technology goes into track mode, becoming soft and flexible for tracking into distal neurovasculature. By applying vacuum, the technology transitions into support mode, maintaining its shape and resists bending.

“SelectFlex™ technology is an important innovation for Q’Apel Medical because it allows us to make catheters that have a mix of trackability and support that is unparalleled in the industry. We can transition from very soft and flexible to highly supportive device on the fly during the case, and it is easily controlled by the user. We look forward to continue differentiating our products through the application of SelectFlex™ technology,” said Jeff Krolik, CTO.

“Our ability to identify unmet clinical needs and build cutting-edge solutions in a timely manner is what differentiates us from our contemporaries. The SelectFlex™ technology plays a huge role in our success and is foundational in our product pipeline,” said King Nelson, CEO.

Q’Apel Medical has other pending patent applications and plans to acquire CE Certification and expand into Europe later this year. Q’Apel Medical products are currently being utilized in over 200 hospital systems nationwide.

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.”