Press Releases

  • Astura Medical Receives FDA 510(k) Clearance For Dolomite Stand-Alone Anterior Cervical Stabilization System

    Authored: November 13, 2020

    Astura Medical, a high-growth, innovative spine technology company, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Dolomite Stand-Alone Anterior Cervical Stabilization System. Expanding on the rapid adoption and recent success of the company’s other integrated plate and spacer technologies for anterior lumbar and lateral lumbar procedures, Dolomite was designed to deliver the widest array of construct options with the most efficient and streamlined supporting instrumentation in the anterior cervical surgery marketplace today. “Even …
  • Astura Medical Receives FDA 510(k) Clearance For El Capitan Lumbar Interbody Fusion System

    Authored: September 23, 2020

    IRVING, TX – April 30, 2020 – Astura Medical, a high-growth, innovative spine technology company, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its El Capitan Anterior Lumbar Interbody Fusion (ALIF) System. El Capitan was designed to provide the widest array of interbody and fixation options, along with the most efficient and streamlined supporting instrumentation on the market today. “With the increased adoption and utility of anterior column reconstruction, we aimed …
  • Astura Medical Receives FDA 510(k) Clearance For SIRION Lateral Lumbar Interbody Fusion System

    Authored: April 16, 2020

    IRVING, TX – April 14, 2020 – Astura Medical, a high-growth, innovative spine technology company, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Sirion Lateral Lumbar Interbody Fusion (LLIF) System. From initial access with the retractor to the interbody and plating options, the Sirion LLIF System delivers unprecedented intraoperative flexibility and efficiency by providing a complete procedural solution for lateral surgery driven by surgeon preference. “Since the outset of the design process, our …
  • Astura Medical Announces New Headquarters in Irving, Texas

    Authored: November 1, 2019

    Astura Medical, a high-growth, innovative spine technology company, today announced the relocation of its corporate headquarters from Carlsbad, California to Irving, Texas, effective November 4, 2019. The company’s new 40,000 square foot facility will provide an expanded framework to support its current growth and future expansion. The company’s operations, including research and development, finance, accounting, marketing, sales, customer service, quality control, shipping/receiving, and professional education, including a new state-of-the-art cadaver lab and training center, will be housed in the new …
  • Astura Medical Announces Partnership with Academy Medical

    Authored: June 4, 2019

    Astura Medical, a high-growth, innovative spine technology company, and Academy Medical, a Service-Disabled Veteran-Owned Small Business (SDVOSB) with priority status with government purchasing agents, today announced their partnership for contracting within the Department of Defense (DoD) and VA. Academy Medical’s goal is to provide sales channels, via contracts, to appropriate medical and surgical vendors, ultimately creating a streamlined, more efficient process for government purchasing agents. Astura Medical’s partnership with Academy Medical will help advance their penetration into the VA and DoD marketplace …
  • Astura Medical Receives FDA 510(k) Clearance For HALF DOME X Expandable Posterior Lumbar Interbody System

    Authored: May 6, 2019

    Astura Medical, a high-growth, innovative spine technology company, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Half Dome X Expandable Posterior Lumbar Interbody System.   The Half Dome X system delivers a new level of intraoperative flexibility and efficiency by providing infinitely adjustable expansion of height and width of the interbody spacer for a controlled restoration of disc height and optimized fit. These features, coupled with acid-etched endplates of the implant and an integrated bone …
  • Astura Medical Reports 104% Annual Revenue Growth in 2018

    Authored: March 25, 2019

    CARLSBAD, CA – March 22, 2019 – Astura Medical, a high-growth, innovative spine technology company, today reported an annual revenue increase of 104% for the full year ending Dec. 31, 2018. “We’re proud of the successful performance by our team in 2018. To more than double our revenue for the third consecutive year further solidifies our position in the marketplace as one of the fastest growing companies in spine today,” said Joel Gambrell, Co-founder & CEO. “The increasing number of our …
  • Astura Medical Perfecting the Art and Science behind Spine Technology

    Authored: January 23, 2019

    The US spinal implant market is currently the largest in the world, standing at $12 billion and estimated to reach $17 billion by 2021. Despite the massive growth rate, when it comes to quality medical device supply, the industry appears to have fallen short outside of the large mainstay players at the top. The increasing complexity of devices, rising cost pressures, and the murky intent of physician-owned distributorships all contribute to the widening gap in optimal product quality and performance. …
  • Astura Medical Receives FDA 510(k) Clearance For OLYMPIC MIS Posterior Spinal Fixation System

    Authored: November 26, 2018

    Astura Medical, a high-growth, innovative spine technology company, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Olympic Minimally Invasive Surgery (MIS) Posterior Spinal Fixation System.   The Olympic MIS system delivers a new level of intraoperative flexibility and efficiency by allowing surgeons to customize to their preferred workflow through the utilization of either a traditional jamshidi/guide wire technique, awl-tap wireless technique, or single-step wireless technique for the placement of MIS pedicle screws. The system features an …
  • Astura Medical Receives FDA 510(k) Clearance For Cervical and Lumbar HA PEEK Interbody Systems

    Authored: June 4, 2018

    Astura Medical, a high growth, innovative spine technology company, today announced that it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its ALTA ACDF Interbody Spacers and HALF DOME Lumbar Interbody Spacers in PEEK-OPTIMA™ HA Enhanced from Invibio Biomaterial Solutions. Combining the clinically proven strength and versatility of PEEK-OPTIMA with Hydroxyapatite (HA), a well-known osteoconductive material that enhances bone apposition, PEEK-OPTIMA HA Enhanced provides an innovative biomaterial for interbody fusion devices. HA is fully integrated, not …