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  • Bacterial Endotoxin Control in Orthopedic Device Manufacturing

    Bacterial endotoxin contamination on orthopedic devices can result in adverse regulatory and patient impact, and considerable product cost. This presentation discusses the types of devices that need to be tested for product release, sources of endotoxin and primary endotoxin test methods.

  • Beyond 3D Printing: ADDITIVE PLUS Revolutionizes Orthopedic Manufacturing

    ADDITIVE PLUS is a framework beyond traditional 3D printing. This session explores Lincotek's integrated suite of services, from Design for AM and advanced high-performance coatings to streamlined post-processing and packaging, delivers significant cost reductions and efficiency improvements.

  • Speeding Innovation Through Streamlined Regulatory Tools

    FDA has new approaches to navigating the complex regulatory landscape and systems in place to remove the burdens of securing marketing clearance for innovative devices that promise to improve patient care.

  • Validation of Orthopedic Devices with Chlorine Dioxide Gas Sterilization

    This presentation discusses chlorine dioxide gas sterilization, the technology and science behind it, and its benefits over other sterilization methods. Through a case study on a knee system, you'll learn about the implementation, validation and effectiveness of the chlorine dioxide process.

  • VOLLMER: Presenting the Future of Deburring

    Ultrasonic deburring is a groundbreaking new process that eliminates the disadvantages of other deburring methods while delivering optimum results without material removal. This presentation demonstrates ultrasonic deburring and shares how it's used on metals and plastics.