KRMD Submits 510(k) to Use FreedomEDGE System With Oncology Biologic

Core Insights - KORU Medical Systems, Inc. (KRMD) has submitted a 510(k) premarket notification to the FDA for its FreedomEDGE infusion system to deliver PHESGO, a breast cancer treatment, subcutaneously instead of intravenously, marking a significant regulatory and strategic milestone for the company [2][5] Company Developments - The FDA clearance submission for FreedomEDGE aligns with KRMD's long-term growth strategy to transition oncology care from intravenous to subcutaneous drug delivery, potentially improving efficiency for infusion centers and easing the workload for nurses [3][7] - The successful clearance and commercialization of the FreedomEDGE system could expand KRMD's addressable market by establishing a subcutaneous delivery platform for oncology biologics, moving beyond its traditional immunology treatments [5][8] - The FreedomEDGE system aims to simplify the treatment process for infusion centers by addressing challenges such as complicated treatment steps and time constraints, thereby enhancing patient comfort and operational efficiency [9][10] Market Context - The subcutaneous drug delivery devices market is projected to be valued at $33.56 billion by 2025, with a CAGR of 7.62% through 2034, driven by the increasing prevalence of chronic diseases and the adoption of subcutaneous delivery devices [11]