Sutura Medical Technology, Inc. is one of 16269 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sutura Medical Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Barbed PDO Suture
1
Total
1
Cleared
0
Denied
Sutura Medical Technology, Inc. has 1 FDA 510(k) cleared medical devices. Based in Dedham, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sutura Medical Technology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Health Policy and Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Sutura Medical Technology, Inc.
1 devices