Suturion AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Suturion AB - FDA 510(k) Cleared Devices
Recent clearances: Suture-TOOL System, Suture-TOOL System
2
Total
2
Cleared
0
Denied
Suturion AB has 2 FDA 510(k) cleared medical devices. Based in Lund, SE.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Suturion AB Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Target Health, LLC and Target Health.
FDA 510(k) Regulatory Record - Suturion AB
2 devices