{"id":974548,"date":"2026-06-23T06:33:19","date_gmt":"2026-06-23T10:33:19","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\/"},"modified":"2026-06-23T06:33:19","modified_gmt":"2026-06-23T10:33:19","slug":"teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\/","title":{"rendered":"Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold"},"content":{"rendered":"<p>        <!--.bwalignc { text-align: center; list-style-position: inside }\n.bwlistdecimal { list-style-type: decimal }body {font:normal small Arial,Helvetica,sans-serif;color:#000;background-color:#fff;padding:24px;margin:0;} a img {border:0;} h3 {font-size:medium;color:#000;margin:0 0 1em 0; text-align:center;}-->  <\/p>\n<p class=\"bwalignc\"><b>Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of <\/b><b>Freesolve\u2122 Resorbable Magnesium Scaffold<\/b><\/p>\n<p class=\"bwalignc\"><i>Enrollment completed ahead of schedule in BIOMAG\u2122-II<\/i><\/p>\n<p class=\"bwalignc\"><i>Positive four-year BIOMAG\u2122-I results recently reported<\/i><\/p>\n<p>WAYNE, Pa.&#8211;(<a href=\"http:\/\/www.businesswire.com\">BUSINESS WIRE<\/a>)&#8211;<br \/>\nTeleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced the beginning of enrollment in the BIOMAG\u2122\u2011III Study (<a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fclinicaltrials.gov%2Fstudy%2FNCT07258290&amp;esheet=54558134&amp;newsitemid=20260623597311&amp;lan=en-US&amp;anchor=NCT07258290&amp;index=1&amp;md5=96a5d16f134012207f98b99e533ba573\">NCT07258290<\/a>), a landmark global study evaluating the Freesolve\u2122 Resorbable Magnesium Scaffold (RMS).<\/p>\n<p><b>Dr. Itsik Ben-Dor<\/b>, MedStar Health in Washington, D.C., is the first implanter in the United States (U.S.) in the IDE trial of Freesolve\u2122 RMS. Designed as a pivotal trial to support future regulatory applications, the BIOMAG\u2122\u2011III Study represents the most comprehensive planned clinical evaluation of Freesolve\u2122 RMS to date.<\/p>\n<p>\nChairman of the steering committee of the BIOMAG\u2122-III Study, <b>Dr. Ron Waksman<sup>\u01c2<\/sup><\/b>, Associate Director of Cardiology at MedStar Washington Hospital Center, stated: \u201cI\u2019m proud that the very first patient in the BIOMAG\u2122-III IDE trial has been enrolled at MedStar Health. Contributing to this important international study is the first step towards potentially changing how we treat narrowed arteries, a very common condition we see in our clinics every day. Researching innovative therapies like Freesolve\u2122 RMS is critical to advancing care for our patients.\u201d<\/p>\n<p>\nThe BIOMAG\u2122-III Study is a randomized controlled trial (RCT). The study will enroll 1,859 patients and compare Freesolve\u2122 RMS to Xience\u2122 Drug\u2011Eluting Stent (DES) with respect to Target Lesion Failure (TLF) rate<sup>a<\/sup> at 12 months. The study will include scaffold lengths up to 40mm. The BIOMAG\u2122-III Study will be conducted at up to 120 sites worldwide, including up to 60 sites in the U.S., underlining Teleflex\u2019s strong global commitment to advancing resorbable scaffold technology.<\/p>\n<p>\nFurthermore, enrollment recently completed ahead of schedule for the BIOMAG\u2122-II Study (<a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fclinicaltrials.gov%2Fstudy%2FNCT05540223%3Fcond%3DNCT05540223%26viewType%3DCard%26rank%3D1&amp;esheet=54558134&amp;newsitemid=20260623597311&amp;lan=en-US&amp;anchor=NCT05540223&amp;index=2&amp;md5=b89e1af5e4f07c19961a74fd0d010d04\">NCT05540223<\/a>). This study enrolled 1,861 patients across 20 countries in Europe and Asia Pacific. The BIOMAG\u2122-II Study is a prospective, international, multi-center, RCT comparing Freesolve\u2122 RMS with Xience\u2122 DES with respect to TLF rate<sup>a<\/sup> at 12 months. Completion of enrollment marks a major milestone for the first large\u2011scale, head\u2011to\u2011head RCT evaluating Freesolve\u2122 RMS against DES.<\/p>\n<p>\nAdditionally, Teleflex recently announced positive long-term data from the BIOMAG\u2122-I First-In-Human (FIH) Study (<a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fclinicaltrials.gov%2Fstudy%2FNCT04157153%3Fterm%3DBIOMAG-I%26rank%3D1&amp;esheet=54558134&amp;newsitemid=20260623597311&amp;lan=en-US&amp;anchor=NCT04157153&amp;index=3&amp;md5=73ebf53af5dbb72ca7c9ffd08d980662\">NCT04157153<\/a>), demonstrating 3.5% TLF<sup>b<\/sup> at four years and no new clinical events between two and four years for Freesolve\u2122 RMS<sup>1<\/sup>.<\/p>\n<p>\n\u201cThe BIOMAG\u2122\u2011III Study represents an important milestone in the evolution of resorbable technologies,\u201d said <b>Dr. David E. Kandzari<sup>\u01c2<\/sup><\/b>, U.S. National Principal Investigator for the BIOMAG\u2122-III Study, Chief, Piedmont Heart Institute, and Chief Scientific Officer, Piedmont Healthcare. \u201cFreesolve\u2122 RMS technology has shown positive outcomes in the BIOMAG\u2122-I FIH trial, with a plateauing of clinical events after resorption. This has long been the vision of resorbable scaffolds.\u201d<\/p>\n<p>\nFreesolve\u2122 RMS is engineered to resorb within 12 months<sup>2<\/sup>, potentially reducing long\u2011term events associated with permanent metallic implants. The BIOMAG\u2122\u2011III Study aims to generate pivotal evidence required to bring this technology to physicians and patients.<\/p>\n<p>\n\u201cThe BIOMAG\u2122\u2011III Study is a pivotal trial designed not only to meet rigorous regulatory standards, but also to demonstrate the long\u2011term safety and efficacy of a fully resorbable magnesium scaffold for patients, physicians, and healthcare systems,\u201d says <b>Prof. Dr. Georg Nollert<\/b>, Vice President Medical Affairs at Teleflex. \u201cWe believe Freesolve\u2122 RMS has the potential to reshape the coronary intervention landscape, and the BIOMAG\u2122\u2011III Study could be the catalyst to drive that.\u201d<\/p>\n<p><b>About Teleflex Incorporated<br \/>\n<br \/><\/b>As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people\u2019s lives. Through our vision to become the most trusted partner in the world of healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose driven innovation, and world-class products can shape the future direction of healthcare.<\/p>\n<p>\nTeleflex is the home of Arrow\u2122, Barrigel\u2122, Deknatel\u2122, LMA\u2122, Pilling\u2122, QuikClot\u2122, R\u00fcsch\u2122, UroLift\u2122 and Weck\u2122 \u2013 trusted brands united by a common sense of purpose.<\/p>\n<p>\nAt Teleflex, we are empowering the future of healthcare. For more information, please visit <a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=http%3A%2F%2Fwww.teleflex.com&amp;esheet=54558134&amp;newsitemid=20260623597311&amp;lan=en-US&amp;anchor=teleflex.com&amp;index=4&amp;md5=309e19e9d4d41f9d5ba195560766414c\">teleflex.com<\/a>.<\/p>\n<p><b>Forward-Looking Statements<br \/>\n<br \/><\/b>Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements. Any forward-looking statements contained herein are based on our management&#8217;s current beliefs and expectations, but are subject to a number of risks, uncertainties and changes in circumstances, which may cause actual results or company actions to differ materially from what is expressed or implied by these statements. These risks and uncertainties are identified and described in more detail in our filings with the Securities and Exchange Commission, including our Annual Report on Form 10-K.<\/p>\n<p><i>Teleflex, the Teleflex logo, Arrow, Barrigel, BIOMAG, Deknatel, Freesolve, LMA, Pilling, QuikClot, R\u00fcsch, UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates in the U.S. and\/or other countries. All other trademarks marked with a \u2122 are the property of their respective owners and are solely used for identification purposes and do not imply any affiliation, endorsement, or ownership by Teleflex Incorporated or its affiliates. Information in this material is not a substitute for the product Instructions for Use. Not all products may be available in all countries.<br \/>\n<br \/><\/i><i>\u00a9 2026 Teleflex Incorporated. All rights reserved. MC-012134 Rev 0.<\/i><\/p>\n<p><b>References:<\/b><\/p>\n<ol class=\"bwlistdecimal\">\n<li>\nTorzewski, J. Lessons from the long-term DES data: how they can inform today&#8217;s practice &#8211; BIOMAG-I: 4-Year Clinical Outcomes of the Resorbable Magnesium Scaffold-DREAMS 3G. pcronline.com Published May 20, 2026. Accessed June 3, 2026. <a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.pcronline.com%2FCases-resources-images%2FResources%2FCourse-videos-slides%2F2026%2FEuroPCR%2FLessons-from-the-long-term-DES-data-how-they-can-inform-today-s-practice%3Fauth%3Dtrue&amp;esheet=54558134&amp;newsitemid=20260623597311&amp;lan=en-US&amp;anchor=https%3A%2F%2Fwww.pcronline.com%2FCases-resources-images%2FResources%2FCourse-videos-slides%2F2026%2FEuroPCR%2FLessons-from-the-long-term-DES-data-how-they-can-inform-today-s-practice%3Fauth%3Dtrue&amp;index=5&amp;md5=6a043999ededfd8485b44ba55488f11f\">https:\/\/www.pcronline.com\/Cases-resources-images\/Resources\/Course-videos-slides\/2026\/EuroPCR\/Lessons-from-the-long-term-DES-data-how-they-can-inform-today-s-practice?auth=true<\/a>. Research sponsored by Teleflex.<\/p>\n<\/li>\n<li>\nSeguchi, M., Aytekin, A., Xheoa, E. et al. Vascular response following implantation of the third-generation drug-eluting resorbable coronary magnesium scaffold: an intravascular imaging analysis of the BIOMAG-I first-in-human study. <i>EuroIntervention.<\/i> 2024; 20(18): e1173-e1183. doi: 10.4244\/EIJ-D-24-00055. Scaffold 99.0% resorbed at 12 months (markers are not resorbable). Research sponsored by Teleflex.<\/p>\n<\/li>\n<\/ol>\n<p><b>Disclaimers<\/b>:<\/p>\n<p><sup>a <\/sup>For BIOMAG\u2122-III and BIOMAG\u2122-II Studies, TLF is a composite of Cardiac Death, Target Vessel Q-wave or non-Q wave Myocardial Infarction, or clinically driven Target Lesion Revascularization (TLR).<br \/>\n<br \/><sup>b <\/sup>For BIOMAG\u2122-I<sup \/>Study, TLF is a composite of Target-Vessel Myocardial Infarction (TV-MI), clinically driven Target Lesion Revascularization (CD-TLR) and Cardiac Death. BIOMAG\u2122-I FIH Study data is based on Kaplan-Meier failure estimate analysis.<\/p>\n<p><sup>\u01c2<\/sup>Drs. Waksman and Kandzari are paid consultants of Teleflex.<\/p>\n<p>\nCAUTION\u2014Investigational device. Limited by the United States law to investigational use.<br \/>\n<br \/>Freesolve\u2122 RMS is clinically often referred to as DREAMS 3G RMS.<br \/>\n<br \/>Freesolve\u2122 RMS is not approved for sale in the United States and is commercially available in CE-mark accepting countries only. Indications for Use may vary by geographic location.<\/p>\n<p><img decoding=\"async\" alt=\"\" src=\"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&amp;sty=20260623597311r1&amp;sid=flmnd&amp;distro=nx&amp;lang=en\" style=\"width:0;height:0\" \/><span class=\"bwct31415\" \/><\/p>\n<p id=\"mmgallerylink\"><span id=\"mmgallerylink-phrase\">View source version on businesswire.com: <\/span><span id=\"mmgallerylink-link\"><a href=\"https:\/\/www.businesswire.com\/news\/home\/20260623597311\/en\/\" rel=\"nofollow\">https:\/\/www.businesswire.com\/news\/home\/20260623597311\/en\/<\/a><\/span><\/p>\n<p>\nTeleflex<br \/>\n<br \/>Lawrence Keusch<br \/>\n<br \/>Vice President, Investor Relations and Strategy Development<br \/>\n<br \/><a rel=\"nofollow\" href=\"mailto:investor.relations@teleflex.com\">investor.relations@teleflex.com<br \/>\n<\/a><br \/>610-948-2836<\/p>\n<p><b>KEYWORDS:<\/b> United States North America Pennsylvania<\/p>\n<p><b>INDUSTRY KEYWORDS:<\/b> Health Medical Devices Surgery Health Technology Clinical Trials Cardiology Biotechnology<\/p>\n<p><b>MEDIA:<\/b><\/p>\n<table cellpadding=\"3\" cellspacing=\"3\">\n<tr>\n<td><font face=\"Arial\" size=\"2\"><b>Logo<\/b><\/font><\/td>\n<\/tr>\n<tr>\n<td><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20260623597311\/en\/2710168\/3\/Teleflex_Global_Corporate_Brand_Logo_CMYK_Navy-White_%28002%29.jpg\" alt=\"Logo\" \/><\/td>\n<\/tr>\n<tr>\n<td><font face=\"Arial\" size=\"2\"><\/font><\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"<p>Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold Enrollment completed ahead of schedule in BIOMAG\u2122-II Positive four-year BIOMAG\u2122-I results recently reported WAYNE, Pa.&#8211;(BUSINESS WIRE)&#8211; Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced the beginning of enrollment in the BIOMAG\u2122\u2011III Study (NCT07258290), a landmark global study evaluating the Freesolve\u2122 Resorbable Magnesium Scaffold (RMS). Dr. Itsik Ben-Dor, MedStar Health in Washington, D.C., is the first implanter in the United States (U.S.) in the IDE trial of Freesolve\u2122 RMS. Designed as a pivotal trial to support future regulatory applications, the BIOMAG\u2122\u2011III Study represents the most comprehensive planned clinical evaluation of Freesolve\u2122 RMS to date. Chairman of the steering committee of the BIOMAG\u2122-III Study, &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-974548","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold Enrollment completed ahead of schedule in BIOMAG\u2122-II Positive four-year BIOMAG\u2122-I results recently reported WAYNE, Pa.&#8211;(BUSINESS WIRE)&#8211; Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced the beginning of enrollment in the BIOMAG\u2122\u2011III Study (NCT07258290), a landmark global study evaluating the Freesolve\u2122 Resorbable Magnesium Scaffold (RMS). Dr. Itsik Ben-Dor, MedStar Health in Washington, D.C., is the first implanter in the United States (U.S.) in the IDE trial of Freesolve\u2122 RMS. Designed as a pivotal trial to support future regulatory applications, the BIOMAG\u2122\u2011III Study represents the most comprehensive planned clinical evaluation of Freesolve\u2122 RMS to date. Chairman of the steering committee of the BIOMAG\u2122-III Study, &hellip; Continue reading &quot;Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2026-06-23T10:33:19+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&amp;sty=20260623597311r1&amp;sid=flmnd&amp;distro=nx&amp;lang=en\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"6 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold\",\"datePublished\":\"2026-06-23T10:33:19+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\\\/\"},\"wordCount\":1164,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/cts.businesswire.com\\\/ct\\\/CT?id=bwnews&amp;sty=20260623597311r1&amp;sid=flmnd&amp;distro=nx&amp;lang=en\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\\\/\",\"name\":\"Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold - 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Market Newsdesk","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.marketnewsdesk.com\/index.php\/teleflex-initiates-enrollment-in-global-biomag-iii-pivotal-trial-of-freesolve-resorbable-magnesium-scaffold\/","og_locale":"en_US","og_type":"article","og_title":"Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold - Market Newsdesk","og_description":"Teleflex Initiates Enrollment in Global BIOMAG\u2122\u2011III Pivotal Trial of Freesolve\u2122 Resorbable Magnesium Scaffold Enrollment completed ahead of schedule in BIOMAG\u2122-II Positive four-year BIOMAG\u2122-I results recently reported WAYNE, Pa.&#8211;(BUSINESS WIRE)&#8211; Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced the beginning of enrollment in the BIOMAG\u2122\u2011III Study (NCT07258290), a landmark global study evaluating the Freesolve\u2122 Resorbable Magnesium Scaffold (RMS). Dr. Itsik Ben-Dor, MedStar Health in Washington, D.C., is the first implanter in the United States (U.S.) in the IDE trial of Freesolve\u2122 RMS. Designed as a pivotal trial to support future regulatory applications, the BIOMAG\u2122\u2011III Study represents the most comprehensive planned clinical evaluation of Freesolve\u2122 RMS to date. 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