East End Medical I, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
East End Medical I, LLC - FDA 510(k) Cleared Devices
Recent clearances: SafeCross Vascular Introducer System (4001), SafeCross Transseptal Puncture and Introducer (TSP/I) System
2
Total
2
Cleared
0
Denied
East End Medical I, LLC has 2 FDA 510(k) cleared medical devices. Based in Sunrise, US.
Latest FDA clearance: Sep 2024. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by East End Medical I, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mandell Horwitz Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - East End Medical I, LLC
2 devices