Saluda Medical Receives Regulatory Approval for EVA™ Sensing Technology in Europe with recognition in Australia

EVA Sensing Technology automates manual programming steps and objectively scans and analyzes a patient's spinal cord to deliver therapy with optimized precision. By removing clinical guesswork and anchoring therapy to each patient's unique spinal cord physiology, EVA Sensing Technology sets a new standard for personalized pain management.

"This approval is in line with our expectations and builds on the successful commercialization we've seen in the U.S., this expansion allows us to bring a proven technology enhancement to more markets," said Barry Regan, CEO, Saluda Medical. "This reinforces our commitment to driving innovation and improving outcomes for patients worldwide."

"EVA Sensing Technology builds on the positive outcomes we have seen with the Evoke® System's closed-loop therapy compared to traditional SCS," Harold Nijhuis, MD, Pain Specialist, Antonius Hospital, Netherlands. "It delivers objective neural metrics aligned with maximum analgesic benefit while streamlining programming to improve efficiency and enhancing the patient experience."

A limited commercial release in Europe and Australia will begin in the first calendar quarter of 2026, followed by a full commercial release later in the year. The timing of this approval and launch is in line with the Company's internal expectations.

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About Saluda Medical
Saluda Medical is a commercial-stage medical device company focused on developing treatments for chronic neurological conditions using its novel neuromodulation platform. The Company's closed-loop, dose-control platform senses and measures neural responses to stimulation and automatically adjusts therapy based on real-time neurophysiological feedback. The Company's first product, the Evoke® System, is indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs, including unilateral or bilateral pain associated with failed back surgery syndrome, intractable low back pain, and leg pain, and is designed to treat chronic neuropathic pain by providing spinal cord stimulation (SCS) therapy that senses and measures neural activation to optimize therapy and reduce patient and clinician burden. 12-month results from the EVOKE study, the first and only prospective, multi-center, parallel-arm, double blind, randomized controlled pivotal study with a voluntary crossover arm in SCS, that demonstrated clinically superior pain relief to open-loop therapy, were published in The Lancet Neurology, 24-month results were published in JAMA Neurology, and 36-month data, that demonstrated sustained pain relief, were published in Regional Anesthesia and Pain Medicine. To learn more, including risks and important safety information, visit  www.saludamedical.com/us/safety/.

Foreign Ownership Restriction

Saluda's CHESS Depositary Interests (CDIs) are issued in reliance on Regulation S under the U.S. Securities Act of 1933, as amended (the U.S. Securities Act), and a no-action letter issued by the staff of the U.S. Securities and Exchange Commission. Accordingly, the Company's CDIs have not been, and will not be, registered under the U.S. Securities Act (except pursuant to an effective registration statement) or the securities laws of any state or other jurisdiction in the United States. The holders of Saluda's CDIs may not offer, sell, pledge, or otherwise transfer the CDIs into the United States or to, or for the account or benefit of, a "U.S. Person" (as defined in Rule 902(k) of Regulation S under the U.S. Securities Act) for a period of at least 12 months from the allotment date under the IPO, unless the resale of the CDIs is registered under the U.S. Securities Act or an exemption from registration is available.

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SOURCE Saluda Medical