{"version":"1.0","provider_name":"Ed Egan","provider_url":"https:\/\/www.edegan.com\/articles","title":"Medical Device Startups and the FDA - Ed Egan","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"Lo9phn8a0E\"><a href=\"https:\/\/www.edegan.com\/articles\/medical-device-startups-and-the-fda\/\">Medical Device Startups and the FDA<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.edegan.com\/articles\/medical-device-startups-and-the-fda\/embed\/#?secret=Lo9phn8a0E\" width=\"600\" height=\"338\" title=\"&#8220;Medical Device Startups and the FDA&#8221; &#8212; Ed Egan\" data-secret=\"Lo9phn8a0E\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script>\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n<\/script>\n","thumbnail_url":"https:\/\/www.edegan.com\/articles\/wp-content\/uploads\/2017\/04\/EDK_Pump_1.jpg","thumbnail_width":2146,"thumbnail_height":3272,"description":"Does the FDA approval process impede innovation?\u00a0Medical devices must be reviewed for\u00a0safety and effectiveness by the Food and Drug Administration\u00a0before being marketed in\u00a0United States, which encompasses\u00a043 percent of the global market for medical devices.\u00a0Startups in the medical device industry are often dissatisfied with this approval process, favoring the FDA&#8217;s\u00a0European Union peer, CE Marking. Some founders\u00a0even&hellip;"}