The new CPT code reflects the latest efficacious medical care available to patients, facilitating adoption and utilization.The assignment of a Category I CPT® code demonstrates a strong message to payers, both commercial and government, that there is now a path to consistent reporting and reimbursement for providers in the medical community. CARMEL, Ind., Jan. 08, 2026 (GLOBE NEWSWIRE) -- NeurAxis, Inc. (“NeurAxis” or the “Company”) (NYSE American: NRXS), a medical technology company commercializing neuromo ...

Core Insights - Aurora Spine Corporation has announced the issuance of two new U.S. patents, enhancing its intellectual property portfolio and supporting its long-term innovation strategy in spinal implants [1][4]. Patent Details - The first patent, No. 12,478,411 B2, titled "Spinal Implant for Motion Preservation or Fusion," is the tenth patent for the ZIP™ implant family, expanding the protected design space of this clinically adopted platform [2][3]. - The second patent, No. 12,478,481 B2, focuses on "Bone Density Scan Result-Matched Orthopedic Implants," which allows for the selection of orthopedic implants based on a patient's bone density scan results [4][5]. Technological Innovations - The patented spinal implant architecture supports either motion preservation or fusion, utilizing multiple structural components to distribute load and engage progressively under physiological forces, addressing limitations of traditional rigid implants [3]. - The bone density scan technology establishes a structured, data-driven framework for surgeons to align implant selection with patient bone characteristics, enhancing the decision-making process in spine surgery [6]. Strategic Implications - The issuance of these patents underscores Aurora Spine's commitment to diverse innovation pathways, supporting future product development and reinforcing the company's reputation for meaningful, surgeon-driven innovation [6]. - The patents are now enforceable in the United States, further solidifying the company's competitive position in the market [7].

Leadership Changes - Teleflex Incorporated has appointed Stuart Randle as Interim President and CEO, succeeding Liam Kelly, who has stepped down from his roles [1] - Stephen Klasko has been appointed as Chairman of the Board [1][2] Revenue Outlook - The company has lowered its full-year revenue outlook for 2025 to a range of $3.270 billion to $3.278 billion, down from the previous guidance of $3.305 billion to $3.320 billion [3] - The revision is attributed to softer-than-expected demand for intra-aortic balloon pumps and catheters in the U.S. and Asia, delays in certain OEM purchase orders, and lower overall order volumes across parts of its portfolio [3] Strategic Focus - Teleflex is transitioning to a more focused, higher-growth organization following the announced sale of its Acute Care, Interventional Urology, and OEM businesses [3] - The Board believes this leadership transition is timely to best position the company for future growth [3]

Company Overview - VolitionRx is focused on saving lives and improving outcomes through low-cost testing in cancer, sepsis, and veterinary applications[4, 5] - The company operates with a low capex, low opex business model, emphasizing commercial partnerships and out-licensing[21] - VolitionRx leverages its IP Powerhouse with 56 patent families and a team with hundreds of years of experience[5] Commercialization and Licensing - The company received $10 million upfront and $13 million in milestone payments from an exclusive Element i+ in-house analyzer licensing partnership[29] - In 2024, Volition sold over 120,000 Nu.Q® Vet Cancer Tests & Components[40] - The company is targeting multiple licensing deals in the human space in 2026, focusing on upfront, milestone, and recurring revenue[25] Products and Market - Nu.Q® Vet is available in the United States, Europe, and Asia, detecting 76% of systemic cancers at 97% specificity[38, 40] - The company estimates a $170 million non-regulated animal testing licensing market, a $4 billion lab-developed screening/management market, and a >$3 billion ICU/ED CE Mark/FDA NETosis sales & licensing market[36] - Lung cancer screening and disease management with Nu.Q® is forecasted to reach over 3 million tests by 2035[63]

Leadership Changes - Stuart Randle has been appointed as Interim President and CEO of Teleflex, succeeding Liam Kelly, who has departed from the company [1] - Dr. Stephen Klasko has been appointed as Chairman of the Board [1][2] - The Board has engaged Spencer Stuart to assist in the search for a permanent CEO [2] Business Strategy and Focus - Teleflex is transitioning to a more focused, higher-growth organization following the announced sale of its Acute Care, Interventional Urology, and OEM businesses [3] - The leadership transition is aimed at positioning the company for future growth in core critical care and high-acuity hospital markets [3] Financial Performance Update - The company expects full year 2025 revenue to be between $3.270 billion and $3.278 billion, a decrease from previous guidance of $3.305 billion to $3.320 billion [4] - The revenue reduction is primarily due to lower than expected demand for intra-aortic balloon pumps and catheters in the U.S. and Asia, as well as delays in OEM purchase orders [5] Future Reporting - Teleflex plans to report its full fourth quarter and full year 2025 financial results in late February or early March 2026 [7]

Boston Scientific Corporation (BSX), headquartered in Marlborough, Massachusetts, develops, manufactures, and markets medical devices for use in various interventional medical specialties globally. With a market cap of $140.4 billion, the company’s products are used in interventional cardiology, cardiac rhythm management, peripheral interventions, electrophysiology, neurovascular intervention, endoscopy, and more. The medTech giant is expected to announce its fiscal fourth-quarter earnings for 2025 before ...

Summary of Key Points from the Conference Call Industry Overview - **Industry**: China Healthcare - **Outlook**: The healthcare industry is expected to experience growth driven by supportive policies, innovation, and the expansion of commercial insurance, which will create a sustainable growth environment starting in 2026 [1][2][10]. Core Insights and Arguments 1. **Speculative Rally and Fundamentals**: The rally in the first half of 2025 was driven by speculators, but long-term investors are returning due to improved fundamentals in the second half of 2025 [1]. 2. **Commercial Insurance Expansion**: The commercial health insurance market is projected to expand significantly, potentially covering 30% of national direct medical expenditures, which could lead to a 3-5x growth in the domestic innovative drug market [2][9][10]. 3. **Government Support for Biopharma**: The Chinese government is positioning biopharma as a strategic pillar industry, with initiatives like the National Venture Fund of Rmb100 billion to support innovative drug development [2][17]. 4. **Bio-manufacturing Growth**: China's bio-manufacturers are expected to strengthen their market position due to favorable US/China policies and increased clinical trial activities [3][54]. 5. **Medtech Expansion**: Medtech leaders are anticipated to grow through product upgrades and overseas market expansion, with companies like Mindray and MicroPort Scientific being key beneficiaries [4]. 6. **Impact of DRG Policies**: The worst impacts of Diagnosis-Related Group (DRG) policies are expected to be over, with hospitals likely to see revenue recovery starting in the second half of 2025 [6]. 7. **AI Integration in Healthcare**: Larger hospitals are budgeting significant amounts for AI technologies, which is expected to benefit online healthcare platforms [5]. Additional Important Insights 1. **Clinical Trial Growth**: There has been a notable increase in clinical trial numbers in China, particularly for innovative drugs, which is expected to continue into 2026 [59][60]. 2. **Prescription Trends**: A significant shift is occurring in prescription patterns, with generics dominating public prescriptions and online platforms benefiting from prescription outflow [65][70]. 3. **Investment in Innovative Drugs**: The financing for innovative drugs in China has seen a substantial increase, with total financing reaching Rmb102.6 billion in 2025, marking a 38% increase [43]. 4. **Geopolitical Considerations**: There are minimal concerns regarding the geopolitical landscape affecting the biotech sector, although the upcoming announcement of the 1260H list may cause short-term volatility [64]. Top Investment Picks - **Pharma/Biotech**: Hengrui, Ascletis, Abbisco, Wuxi Apptec, Tigermed, Hygeia, SSY, AliHealth, Yidu Tech [2][3][4][5][6][10]. - **Medtech**: Mindray, United Imaging, MicroPort Scientific [4]. This summary encapsulates the key points discussed in the conference call, highlighting the growth potential and strategic shifts within the China healthcare industry.

Core Viewpoint - Conavi Medical Corp. is conducting a public offering of common shares and pre-funded common share purchase warrants to raise between $12 million and $15 million for regulatory clearance and market release of its Novasight Hybrid system, along with working capital needs [2][3][6]. Group 1: Offering Details - The offering consists of a minimum of 26,666,667 and a maximum of 33,333,333 securities priced at $0.45 per common share or $0.44999 per pre-funded warrant [2]. - Each pre-funded warrant allows the holder to acquire one common share at an exercise price of $0.00001, with no expiration and can be exercised on a cashless basis [2]. - The offering may be completed in one or more tranches, with an expected initial closing date around January 13, 2026, subject to regulatory approvals [6]. Group 2: Use of Proceeds - The net proceeds from the offering will be used to obtain US FDA 510(k) clearance for the Novasight Hybrid system and to facilitate a targeted market release in the United States [3]. - Additional proceeds will be allocated for working capital and general corporate purposes [3]. Group 3: Agent and Fees - The company will pay the agent, Bloom Burton Securities Inc., a cash fee of 6.5% of the gross proceeds and grant compensation options equal to 6.5% of the total number of securities issued [7]. - A reduced cash commission of 3.25% will apply for certain purchasers on a president's list, with no compensation options for those sales [7]. Group 4: Regulatory Filings - An amended and restated final short form prospectus was filed on January 7, 2026, with securities regulatory authorities in Alberta, British Columbia, and Ontario [5]. - The offering is subject to customary closing conditions, including necessary regulatory and stock exchange approvals [6]. Group 5: Company Overview - Conavi Medical focuses on designing, manufacturing, and marketing imaging technologies for minimally invasive cardiovascular procedures [12]. - The Novasight Hybrid system combines intravascular ultrasound and optical coherence tomography into a single device, enabling simultaneous imaging of coronary arteries [12].

Core Viewpoint - Conavi Medical Corp. is conducting a public offering of common shares and pre-funded common share purchase warrants to raise between $12 million and $15 million for regulatory clearance and market release of its Novasight Hybrid system, along with working capital needs [2][3]. Offering Details - The offering consists of a minimum of 26,666,667 and a maximum of 33,333,333 securities priced at $0.45 per common share or $0.44999 per pre-funded warrant [2]. - Each pre-funded warrant allows the holder to acquire one common share at an exercise price of $0.00001, with no expiration and can be exercised on a cashless basis [2]. Use of Proceeds - The net proceeds from the offering will be used to obtain US FDA 510(k) clearance for the Novasight Hybrid system and to support a targeted market release in the United States, as well as for working capital and general corporate purposes [3]. Regulatory and Closing Information - The offering is expected to close on or about January 13, 2026, subject to customary closing conditions and necessary regulatory approvals [6]. - An amended and restated final short form prospectus was filed on January 7, 2026, which must be approved before any sale of securities [5]. Agent Compensation - The company will pay the agent a cash fee of 6.5% of the gross proceeds and grant compensation options equal to 6.5% of the total number of securities issued [7]. - A reduced cash commission of 3.25% will apply for certain purchasers on a president's list, with no compensation options for those sales [7]. Company Overview - Conavi Medical focuses on designing, manufacturing, and marketing imaging technologies for minimally invasive cardiovascular procedures, with its Novasight Hybrid system being the first to combine intravascular ultrasound and optical coherence tomography [12].

Company Overview - Avanos Medical, Inc. is a medical technology company focused on delivering clinically superior medical device solutions to help patients return to their daily activities [2] - The company is headquartered in Alpharetta, Georgia, and is committed to addressing significant healthcare needs, including providing nutrition support for patients transitioning from hospital to home and reducing opioid use during recovery [2] - Avanos develops, manufactures, and markets recognized brands globally, holding leading market positions across multiple categories in its portfolio [2] Upcoming Event - Dave Pacitti, the CEO of Avanos Medical, will present at the 44th Annual J.P. Morgan Healthcare Conference in San Francisco on January 13 at approximately 2:15 p.m. PST [1] - A webcast of the conference presentation will be available on the Investors section of the Avanos Medical website and will be archived for future access [1]