增材制造技术进展及其医学应用

A.J.F. Bastin, Xiao Huang
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引用次数: 1

摘要

增材制造(AM),也被称为三维(3D)打印,是一项颠覆性技术,正在给许多行业带来革命性的变化。它正在获得相当大的关注,特别是在医疗领域,因为它使制造新装置或修改现有装置成为可能,以配合病人的解剖结构,并产生解剖学上精确的模型,支持卫生专业人员进行诊断和手术准备。此外,增材制造的自由形式构建能力使设计师能够完全控制设备的内部结构,以及定制的机械性能,如抗压强度、刚度和许多表面特征。随着AM工艺的深入了解,对打印部件的一致性和质量有了更多的控制,将这项技术定位于医疗应用。随着越来越多的医学批准的3d打印设备进入市场,本文的目的是概述食品和药物管理局批准医疗设备的监管途径,以及医疗行业中使用的常见增材制造工艺。综上所述,将重点介绍增材制造技术和相关公司所支持的医疗设备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progress of Additive Manufacturing Technology and Its Medical Applications
Additive manufacturing (AM), also known as three-dimensional (3D) printing, is a disruptive technology that is revolutionizing many industries. It is gaining considerable attention, particularly in the medical field as it renders the possibilities of building new devices or modifying existing devices to match a patient's anatomy and to produce anatomically exact models, supporting health professionals with diagnostics and surgery preparation. In addition, the free-form building capability of AM allows the designer to have a complete control over the internal architecture of the device, along with tailored mechanical properties, such as compression strength, stiffness, and many surface features. As the processes of AM become well-understood, there is more control over the consistency and quality of the printed parts, positioning this technology for medical applications. With more and more medically approved 3D-printed devices entering the market, the purpose of this paper is to give an overview of the regulatory pathway to the Food and Drug Administration approval of a medical device, along with common AM processes used in the medical industry. To conclude, medical devices that are enabled by AM technology and associated companies will be highlighted.
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