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FDA Premarket Approval Granted for DT MedTech’s Hintermann Series H3™ Total Ankle Replacement System

June 5, 2019 (Baltimore, MD) – DT MedTech, LLC (DTM) announced today that the Hintermann Series H3™ (H3) Total Ankle Replacement (TAR) System has received premarket approval (PMA) from the U.S. Food and Drug Administration. The H3 is a three-piece, mobile-bearing implant. The Hintermann Series H3 Total Ankle Replacement System is indicated for use as …

Ignite Orthopedics Announces First 510(k) Clearance and Company’s Surgeon Development Team

WARSAW, IND. (PRWEB) JUNE 04, 2019 Ignite Orthopedics LLC, a privately held product development and commercialization organization located in the “Orthopedic Capital of the World,” Warsaw, Indiana, announced that it has received FDA clearance to market its Radial Head Arthroplasty System. This marks the first FDA clearance for the company and represents a significant milestone in …

HD LifeSciences Announces Milestone of 1,500th Implant Used

HD LifeSciences, an innovative manufacturer of the only spinal interbody technology that offers a Soft Titanium™ structural lattice, announces the successful implant of the 1,500th cage since the formation of the company in late 2017. Surgeons around the country have complimented the technology for its design and ease of use along with its novel characteristics. …

Demand for Knee Replacement Grows 5 Percent Worldwide

ST. LOUIS, June 4, 2019 /PRNewswire/ — Approximately 40 percent of the global population over age 55 experiences chronic knee pain. Of those, 50.8 million suffer from disabling pain, and about 2.6 million turn to knee replacement surgery each year.  Knee replacement surgery has become more prevalent in recent years due to increased access to orthopedic care in …

Zavation Gains US FDA Clearance for the Ti3Z Interbody System (TLIF, T-PLIF, and PLIF)

FLOWOOD, Miss., June 4, 2019 /PRNewswire/ — Zavation, an employee-owned medical device company that designs, develops, manufactures and distributes medical device products, announced today that it has received 510(k) clearance from the US Food and Drug Administration (FDA) to market the Ti3Z Interbody System (TLIF, T-PLIF, and PLIF).  The Mississippi company will commence launching Ti3Z Interbody system immediately to the US …

Astura Medical Announces Partnership with Academy Medical

CARLSBAD, CA – 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 …

Turnkey Grinding Solutions Provider, Glebar, Bolsters Executive Team with Appointment of New CEO Robert Baker, Formerly of Stryker Corporation

RAMSEY, N.J., June 3, 2019 /PRNewswire/ — Manufacturer and solutions provider of fully automated centerless and other types of turnkey precision grinding systems, Glebar Company, announced today that Robert Baker, formerly of Stryker Corporation, will serve as the new CEO effective June 1, 2019. Former CEO Adam Cook will remain an integral part of the organization’s vision serving as Chairman of the Board. …

Ozop Surgical Corp. Announces Progress on New Spine Implant

WEST PALM BEACH, FL / ACCESSWIRE / June 3, 2019 / Ozop Surgical Corp. (OTCQB: OZSC), a provider of premium surgical devices in the rapidly growing field of minimally invasive spine surgery, today announced significant development progress and completion of initial testing of their novel adjustable ALIF interbody spinal implant. Michael Chermak, CEO, OZOP Surgical commented, …

MiMedx Files Definitive Proxy Materials and Mails Letter to Shareholders

MARIETTA, Ga., June 3, 2019 /PRNewswire/ — MiMedx Group, Inc. (OTC PINK: MDXG) (“MiMedx” or the “Company“), an industry leader in advanced wound care and an emerging therapeutic biologics company, today announced that it has filed definitive proxy materials with the U.S. Securities and Exchange Commission (“SEC“) in connection with its upcoming 2018 annual meeting of shareholders (“Annual …

Smith & Nephew announces completion of Brainlab Orthopaedic Joint Reconstruction Business acquisition

3 June 2019 Smith & Nephew plc (LSE:SN, NYSE:SNN), the global medical technology business, today announces it has completed the acquisition of the Brainlab orthopaedic joint reconstruction business. The acquisition supports Smith & Nephew’s strategy to invest in best-in-class technologies that further its multi-asset digital surgery and robotic ecosystem. The Brainlab orthopaedic joint reconstruction business provides surgeons …

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