{"id":56335,"date":"2023-04-28T14:03:14","date_gmt":"2023-04-28T12:03:14","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/apyx-medical-corporation-receives-fda-510k-clearance-for-the-use-of-renuvion-for-coagulation-of-subcutaneous-soft-tissues-following-liposuction-for-aesthetic-body-contouring\/"},"modified":"2023-04-28T14:03:14","modified_gmt":"2023-04-28T12:03:14","slug":"apyx-medical-corporation-receives-fda-510k-clearance-for-the-use-of-renuvion-for-coagulation-of-subcutaneous-soft-tissues-following-liposuction-for-aesthetic-body-contouring","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/apyx-medical-corporation-receives-fda-510k-clearance-for-the-use-of-renuvion-for-coagulation-of-subcutaneous-soft-tissues-following-liposuction-for-aesthetic-body-contouring\/","title":{"rendered":"Apyx Medical Corporation Receives FDA 510(k) Clearance for the Use of Renuvion\u00ae for Coagulation of Subcutaneous Soft Tissues Following Liposuction for Aesthetic Body Contouring"},"content":{"rendered":"
\n

CLEARWATER, Fla.–(BUSINESS WIRE)–Apyx Medical Corporation (NASDAQ:APYX)<\/b> (the \u201cCompany\u201d), the manufacturer of a proprietary helium plasma and radiofrequency technology marketed and sold as Renuvion\u00ae<\/sup>, today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (\u201cFDA\u201d) for the use of the Renuvion APR Handpiece \u201cfor coagulation of subcutaneous soft tissues following liposuction for aesthetic body contouring.\u201d<\/p>\n

\n\u201cWe are pleased to receive 510(k) clearance for the use of the Renuvion APR Handpiece for coagulation of subcutaneous soft tissues specifically following liposuction for aesthetic body contouring. The Renuvion APR handpiece is the only device to have a 510(k) clearance for use following liposuction\u201d said Charlie Goodwin, President and Chief Executive Officer. \u201cThis 510(k) clearance further demonstrates the safety and effectiveness of our Renuvion technology, and our continued commitment to working with the FDA to secure specific clinical indications.\u201d<\/p>\n

\nMr. Goodwin continued: \u201cWe are proud of the strong progress made by our regulatory and clinical teams to secure clearances supporting the safe and effective use of our Advanced Energy products. Specifically, in the last twelve months we have received four 510(k) clearances for the use of our Renuvion handpieces in specific clinical indications, all of which are supported by substantial evidence demonstrating the safety of our products. Importantly, we believe we now have the requisite 510(k) clearances to resolve the remaining limitations of the FDA Safety Communication. We look forward to empowering surgeons and physicians to obtain the clinical results they, and their patients, are seeking by expanding the adoption and utilization of our Renuvion technology for these specific clinical indications. Moreover, with large and rapidly growing addressable markets that we are just beginning to penetrate, and a dedicated team of employees, we remain excited about our future prospects in the years to come.\u201d<\/p>\n

\nAbout Apyx Medical Corporation<\/span>:<\/b><\/p>\n

\nApyx Medical Corporation is an advanced energy technology company with a passion for elevating people\u2019s lives through innovative products, including its Helium Plasma Technology products marketed and sold as Renuvion in the cosmetic surgery market and J-Plasma\u00ae<\/sup> in the hospital surgical market. Renuvion and J-Plasma offer surgeons a unique ability to provide controlled heat to tissue to achieve their desired results. The Company also leverages its deep expertise and decades of experience in unique waveforms through OEM agreements with other medical device manufacturers. For further information about the Company and its products, please refer to the Apyx Medical Corporation website at www.ApyxMedical.com<\/a>.<\/p>\n

\nCautionary Statement on Forward-Looking Statements<\/span>:<\/b><\/p>\n

\nCertain matters discussed in this release and oral statements made from time to time by representatives of the Company may constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 and the Federal securities laws. Although the Company believes that the expectations reflected in such forward-looking statements are based upon reasonable assumptions, it can give no assurance that its expectations will be achieved.<\/p>\n

\nAll statements other than statements of historical fact are statements that could be deemed forward-looking statements, including but not limited to, any statements regarding the potential impact of the COVID-19 pandemic and the actions by governments, businesses and individuals in response to the situation; projections of net revenue, margins, expenses, net earnings, net earnings per share, or other financial items; projections or assumptions concerning the possible receipt by the Company of any regulatory approvals from any government agency or instrumentality including but not limited to the U.S. Food and Drug Administration, supply chain disruptions, component shortages, manufacturing disruptions or logistics challenges; or macroeconomic or geopolitical matters and the impact of those matters on the Company\u2019s financial performance.<\/p>\n

\nForward-looking statements and information are subject to certain risks, trends and uncertainties that could cause actual results to differ materially from those projected. Many of these factors are beyond the Company\u2019s ability to control or predict. Important factors that may cause the Company\u2019s actual results to differ materially and that could impact the Company and the statements contained in this release include but are not limited to risks, uncertainties and assumptions relating to the regulatory environment in which the Company is subject to, including the Company\u2019s ability to gain requisite approvals for its products from the U.S. Food and Drug Administration and other governmental and regulatory bodies, both domestically and internationally; the impact of the recent FDA Safety Communication on our business and operations; factors relating to the effects of the COVID-19 pandemic; sudden or extreme volatility in commodity prices and availability, including supply chain disruptions; changes in general economic, business or demographic conditions or trends; changes in and effects of the geopolitical environment; liabilities and costs which the Company may incur from pending or threatened litigations, claims, disputes or investigations; and other risks that are described in the Company\u2019s Annual Report on Form 10-K for the fiscal year ended December 31, 2022 and the Company\u2019s other filings with the Securities and Exchange Commission. For forward-looking statements in this release, the Company claims the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995. The Company assumes no obligation to update or supplement any forward-looking statements whether as a result of new information, future events or otherwise.<\/p>\n

Contacts<\/b> <\/p>\n

\nInvestor Relations Contact<\/span>:<\/b>
ICR Westwicke on behalf of Apyx Medical Corporation
\n
Mike Piccinino, CFA
\n
investor.relations@apyxmedical.com<\/a><\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

CLEARWATER, Fla.–(BUSINESS WIRE)–Apyx Medical Corporation (NASDAQ:APYX) (the \u201cCompany\u201d), the manufacturer of a proprietary helium plasma and radiofrequency technology marketed and sold as Renuvion\u00ae, today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (\u201cFDA\u201d) for the use of the Renuvion APR Handpiece \u201cfor coagulation of subcutaneous soft tissues following liposuction for … [Read more…]<\/a><\/span><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":{"0":"entry","1":"post","2":"publish","3":"author-business","4":"post-56335","6":"format-standard","7":"category-industry"},"yoast_head":"\nApyx Medical Corporation Receives FDA 510(k) Clearance for the Use of Renuvion\u00ae for Coagulation of Subcutaneous Soft Tissues Following Liposuction for Aesthetic Body Contouring - Pharma Trend<\/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:\/\/pharma-trend.com\/en\/apyx-medical-corporation-receives-fda-510k-clearance-for-the-use-of-renuvion-for-coagulation-of-subcutaneous-soft-tissues-following-liposuction-for-aesthetic-body-contouring\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Apyx Medical Corporation Receives FDA 510(k) Clearance for the Use of Renuvion\u00ae for Coagulation of Subcutaneous Soft Tissues Following Liposuction for Aesthetic Body Contouring - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"CLEARWATER, Fla.–(BUSINESS WIRE)–Apyx Medical Corporation (NASDAQ:APYX) (the \u201cCompany\u201d), the manufacturer of a proprietary helium plasma and radiofrequency technology marketed and sold as Renuvion\u00ae, today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (\u201cFDA\u201d) for the use of the Renuvion APR Handpiece \u201cfor coagulation of subcutaneous soft tissues following liposuction for ... 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