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    Breaking News

    TendoNova Appoints New CEO

    Atlanta medical device veteran to build a product launch team.

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    Globe Newswire01.08.21
    Atlanta-based TendoNova Corporation has appointed Mark A. Samuels as CEO. Samuels is an experienced Atlanta-based entrepreneur and business leader with a proven track record and multiple successful exits in the medical device industry. TendoNova is an Atlanta-based medical device company that develops devices that enable microinvasive orthopedic procedures. Its initial product, the Ocelot System, addresses chronic tendon pain, a prevalent condition in both athletes and the population at large.
     
    “It is with great pleasure that we welcome Mark Samuels as our new CEO. With the addition of his extensive experience in the medical device industry, to the investment and support of the National Football League Players Association, we believe the company has all the components needed to drive success,” said TendoNova Board Chairman Lou Malice.
     
    Approximately 30 million people in the United States suffer from chronic tendon pain each year. This includes injuries such as tennis elbow, Achilles tendinosis, and patellar tendon pain. These conditions are prevalent in NFL players, weekend warriors, and anyone else who engages in repetitive tasks. If left untreated, chronic tendon pain can lead to months or years of pain and even career-ending injuries.
     
    “I am very excited for the opportunity to join the TendoNova team. The Ocelot technology has the potential to improve tendon treatment worldwide,” Samuels said. “My discussions with potential patients and physicians show a compelling need for improved tendon pain treatment. The Ocelot™ can help meet this need by improving accessibility and physician effectiveness in tendon procedures.”
     
    Prior to joining TendoNova, Samuels was CEO of OBMedical Company for two and a half years. Under his leadership, OBMedical resolved technical and financial issues that had delayed its product launch and grew sales of its advanced fetal monitoring system for women in labor and their babies. Samuels engineered the sale of OBMedical Company to Philips Medical in 2018 for an undisclosed sum and acted as general manager for the company until 2019.
     
    Founded in 2017, TendoNova combines decades of regenerative medicine know-how with modern data analytics to enable in-office procedures to treat chronic tendon pain. The Ocelot System encourages the growth of healthy tendon to replace painful lesions by performing a controlled mechanical debridement of a targeted area. Current methods of treating chronic tendon pain, such as using a needle to poke holes in a tendon, rely heavily on clinician skill and are expensive, invasive, or have inconsistent outcomes. This leaves patients and physicians with limited viable treatment options for patients that fail to heal. TendoNova’s Ocelot System is a smart tool that is easy to use, cost effective, and provides real-time data that enhances the clinician’s skill. By making treatment of chronic tendon pain more accessible and reliable, TendoNova's Ocelot™ System brings surgical level care to the office and training room.
     
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    • Large Joint
      DePuy Synthes Receives 510(k) FDA Clearance for VELYS Robotic-Assisted Solution

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    • OrthoPediatrics Expands Agent Network in Three European Countries

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    • Spine/Neurology
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      Data demonstrate the device’s respect for neural anatomy and conformability to bony endplates through Adaptive Geometry.
      Globe Newswire 01.18.21

    • Large Joint
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      Study shows that an enhanced recovery program leads to optimal results after knee replacement surgery.
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    • Spine/Neurology
      Boston Scientific Releases WaveWriter Alpha Spinal Cord Stimulators in U.S.

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      Full-body MRI conditional devices combine therapy options for personalized pain relief.
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    • New Chief Clinical Officer on Board at IncludeHealth

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      IncludeHealth 01.14.21

    • Imaging
      Cios Flow from Siemen Healthineers Cleared by FDA

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    • CMS Expedites Breakthrough Device Access; Industry Applauds

      CMS Expedites Breakthrough Device Access; Industry Applauds

      New rule creates an accelerated Medicare coverage pathway for innovative products that the FDA deems ‘breakthrough.’
      ODT Staff 01.13.21


    • Biologics
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    • Orthopedic Surgical Robots Market to Exceed $4.1 Billion by 2029

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      Surgical robots associated with advantages such as better visualization of the operating field and lessened tremor.
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    • ARCH Global Precision Acquires LISI Medical Jeropa Inc.

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      Broadens the portfolio of products and end markets served by ARCH.
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    • Large Joint
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    • Extremities
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    Trending
    • DePuy Synthes Receives 510(k) FDA Clearance For VELYS Robotic-Assisted Solution
    • Mini MRI For Hand And Wrist Imaging Can Be Used Nearly Anywhere
    • New Chief Clinical Officer On Board At IncludeHealth
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    • NuVasive XLIF - Minimally Invasive Spine Surgery
    Breaking News
    • Bioventus Appoints SVP of Operations
    • DePuy Synthes Receives 510(k) FDA Clearance for VELYS Robotic-Assisted Solution
    • OrthoPediatrics Expands Agent Network in Three European Countries
    • Studies Show FlareHawk Expandable Cage Delivers Favorable Fusion, Patient Outcomes
    • Rapid Recovery Protocol Can Lead to Increased Range of Motion After TKA
    View Breaking News >
    CURRENT ISSUE

    November/December 2020

    • Making the Grade: Orthopedic Materials Spotlight
    • Mending Mishaps: A Trauma Technology Overview
    • Life, Interrupted: The 2020 Year in Review
    • View More >

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