Iterative Scopes, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iterative Scopes, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SKOUT® system, SKOUT® system, SKOUT® system
4
Total
4
Cleared
0
Denied
Iterative Scopes, Inc. has 4 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Latest FDA clearance: Jul 2024. Active since 2022. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Iterative Scopes, Inc. 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 Scopes, Inc.
4 devices