Iterative Health is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iterative Health - FDA 510(k) Cleared Devices
Recent clearances: SKOUT system, SKOUT system
2
Total
2
Cleared
0
Denied
Iterative Health has 2 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Iterative Health Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Iterative Health
2 devices