Simergent, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Simergent, LLC - FDA 510(k) Cleared Devices
Recent clearances: Archimedes Pro Automated Peritoneal Dialysis Cycler (3014-00000-1)
1
Total
1
Cleared
0
Denied
Simergent, LLC has 1 FDA 510(k) cleared medical devices. Based in Oklahoma City, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Simergent, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Simergent, LLC
1 devices