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      <image:title>Blog - What is a Class III Medical Device?&amp;nbsp; | HaA PD - The United States Food and Drug Administration (FDA) categorize medical devices into three different classes, depending on the level of regulatory control required to maintain both performance and safety. The FDA classifies Class III devices as medical devices that pose the highest risk to both users and patients, requiring the most stringent regulatory oversight. Class III devices are considered higher risk than both Class I and Class II devices due to their intended use and potential impact on patient health. These devices are often life-sustaining, life-supporting, implanted, or critical to preventing serious injury or illness. While Class III devices represent a smaller percentage of all medical devices, they require significantly more regulatory scrutiny, clinical evidence, and development discipline than class I and II devices.</image:title>
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      <image:caption>Insulet Omnipod 2-shot molded chassis components redesigned by HaA PD to simplify electrical connections and reduce manufacturing costs</image:caption>
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      <image:caption>NP Medical nCompass IV catheter with securement surface and 180-degree fluid pathway to reduce kinking and improve stability</image:caption>
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      <image:title>.#6 - Boston Scientific’s Transbronchial System Case Study</image:title>
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