{"id":816777,"date":"2025-02-24T10:40:31","date_gmt":"2025-02-24T15:40:31","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/icecure-submits-filing-for-regulatory-approval-of-its-next-generation-xsense-cryoablation-system-in-israel\/"},"modified":"2025-02-24T10:40:31","modified_gmt":"2025-02-24T15:40:31","slug":"icecure-submits-filing-for-regulatory-approval-of-its-next-generation-xsense-cryoablation-system-in-israel","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/icecure-submits-filing-for-regulatory-approval-of-its-next-generation-xsense-cryoablation-system-in-israel\/","title":{"rendered":"IceCure Submits Filing for Regulatory Approval of its Next-Generation XSense\u2122 Cryoablation System in Israel"},"content":{"rendered":"
\n

PR Newswire<\/p>\n<\/p><\/div>\n

\n

\n
\n Application covering a wide range of indications is in line with trends in de-escalation of surgery and growth in minimally invasive cryoablation procedures, pointing to strong potential for increasing demand\u00a0<\/i>
\n <\/b>\n <\/p>\n

\n
\n CAESAREA, Israel<\/span>
\n <\/span>, Feb. 24, 2025<\/span><\/span> \/PRNewswire\/ — IceCure Medical Ltd.<\/a> (Nasdaq: ICCM) (“IceCure”, “IceCure Medical” or the “Company”), developer of minimally-invasive cryoablation technology that destroys tumors by freezing as an alternative to surgical tumor removal, today announced it has filed for regulatory approval with the Medical Device Division (“AMAR”) of Israel’s<\/span> Ministry of Health for its next-generation single cryoprobe cryoablation system, the XSense\u2122 System and CryoProbes.<\/p>\n

\n \"IceCure\n <\/div>\n

The filing contains a request for approval of all indications for which ProSense\u00ae has already received approval in Israel<\/span>, including general surgery, dermatology, neurology, including cryoanalgesia, thoracic surgery, ENT (ear, nose, throat), gynecology, oncology (including benign and malignant breast tumors), proctology and urology. The Company has already received marketing authorization from the United States Food and Drug Administration (the “FDA”) for the XSense\u2122 System and its cryoprobes.<\/p>\n

“As a leader in liquid-nitrogen based cryoablation technologies, we continue to innovate and bring to market healthcare advancements that support the global move toward de-escalation of surgery and the substantial increase in minimally invasive surgery procedures,” stated IceCure’s Chief Executive Officer, Eyal Shamir<\/span>. “While de-escalation of surgery is a trend specific to the treatment of breast cancer, we see growing opportunities for our cryoablation systems to offer minimally invasive solutions in a wide range and expanding number of indications. We are optimistic about receiving regulatory clearance for XSense\u2122 in Israel<\/span> in the coming months.”<\/p>\n

The global minimally invasive surgery market<\/a> is forecast to grow by a CAGR of 17% between 2022 and 2029 to reach $174 billion<\/span> by 2029.<\/p>\n

\n About IceCure Medical
<\/b>IceCure Medical (Nasdaq: ICCM) develops and markets advanced liquid-nitrogen-based cryoablation therapy systems for the destruction of tumors (benign and cancerous) by freezing, with the primary focus areas being breast, kidney, bone and lung cancer. Its minimally invasive technology is a safe and effective alternative to hospital surgical tumor removal that is easily performed in a relatively short procedure. The Company’s flagship ProSense\u00ae system is marketed and sold worldwide for the indications cleared and approved to date including in the U.S., Europe<\/span>, and China<\/span>.<\/p>\n

\n Forward Looking Statements<\/b>
\n
This press release contains forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995 and other Federal securities laws. Words such as “expects,” “anticipates,” “intends,” “plans,” “believes,” “seeks,” “estimates” and similar expressions or variations of such words are intended to identify forward-looking statements. For example,\u00a0IceCure\u00a0is using forward looking statements in this press release when it discusses: the Company’s view that opportunities for its cryoablation systems are growing in a wide range and expanding number of indications; the impending decision on regulatory clearance for XSense\u2122 in Israel<\/span> by AMAR; and the growth forecast of the global minimally invasive surgery market, pointing to strong potential for increasing demand. Historical results of scientific research and clinical and preclinical trials do not guarantee that the conclusions of future research or trials will suggest identical or even similar conclusions. Important factors that could cause actual results, developments and business decisions to differ materially from those anticipated in these forward-looking statements include, among others: the Company’s planned level of revenues and capital expenditures; the Company’s available cash and its ability to obtain additional funding; the Company’s ability to market and sell its products; legal and regulatory developments in\u00a0the United States\u00a0and other countries; the Company’s ability to maintain its relationships with suppliers, distributors and other partners; the Company’s ability to maintain or protect the validity of its patents and other intellectual property; the Company’s ability to expose and educate medical professionals about its products; political, economic and military instability in the\u00a0Middle East, specifically in\u00a0Israel; as well as those factors set forth in the Risk Factors section of the Company’s Annual Report on Form 20-F for the year ended\u00a0December 31, 2023\u00a0filed with the SEC on\u00a0April 3, 2024, and other documents filed with or furnished to the SEC which are available on the SEC’s website,\u00a0www.sec.gov<\/a>. The Company undertakes no obligation to update these statements for revisions or changes after the date of this release, except as required by law.<\/p>\n

\n IR Contact:
<\/b>
\n Email: <\/span>
\n investors@icecure-medical.com<\/a>
\n
\n Michael <\/span>Polyviou
Phone: 732-232-6914
<\/span>Todd <\/span>Kehrli
Phone: 310-625-4462<\/span><\/p>\n

\n Logo – https:\/\/mma.prnewswire.com\/media\/2319310\/IceCure_Medical_Logo.jpg<\/a><\/span>\n <\/p>\n

\n \"Cision\" View original content:https:\/\/www.prnewswire.com\/news-releases\/icecure-submits-filing-for-regulatory-approval-of-its-next-generation-xsense-cryoablation-system-in-israel-302383227.html<\/a><\/p>\n

SOURCE IceCure Medical<\/p>\n<\/p><\/div>\n

\"\"<\/p>\n","protected":false},"excerpt":{"rendered":"

PR Newswire Application covering a wide range of indications is in line with trends in de-escalation of surgery and growth in minimally invasive cryoablation procedures, pointing to strong potential for increasing demand\u00a0 CAESAREA, Israel , Feb. 24, 2025 \/PRNewswire\/ — IceCure Medical Ltd. (Nasdaq: ICCM) (“IceCure”, “IceCure Medical” or the “Company”), developer of minimally-invasive cryoablation technology that destroys tumors by freezing as an alternative to surgical tumor removal, today announced it has filed for regulatory approval with the Medical Device Division (“AMAR”) of Israel’s Ministry of Health for its next-generation single cryoprobe cryoablation system, the XSense\u2122 System and CryoProbes. The filing contains a request for approval of all indications for which ProSense\u00ae has already received approval in Israel, including general … <\/p>\n

Continue reading “IceCure Submits Filing for Regulatory Approval of its Next-Generation XSense\u2122 Cryoablation System in Israel”<\/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-816777","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nIceCure Submits Filing for Regulatory Approval of its Next-Generation XSense\u2122 Cryoablation System in Israel - 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\/icecure-submits-filing-for-regulatory-approval-of-its-next-generation-xsense-cryoablation-system-in-israel\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"IceCure Submits Filing for Regulatory Approval of its Next-Generation XSense\u2122 Cryoablation System in Israel - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"PR Newswire Application covering a wide range of indications is in line with trends in de-escalation of surgery and growth in minimally invasive cryoablation procedures, pointing to strong potential for increasing demand\u00a0 CAESAREA, Israel , Feb. 24, 2025 \/PRNewswire\/ — IceCure Medical Ltd. (Nasdaq: ICCM) (“IceCure”, “IceCure Medical” or the “Company”), developer of minimally-invasive cryoablation technology that destroys tumors by freezing as an alternative to surgical tumor removal, today announced it has filed for regulatory approval with the Medical Device Division (“AMAR”) of Israel’s Ministry of Health for its next-generation single cryoprobe cryoablation system, the XSense\u2122 System and CryoProbes. 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