Cypris Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cypris Medical - FDA 510(k) Cleared Devices
Recent clearances: Cypris eXact Suture Placement Device, Cypris eXact Suturing System
2
Total
2
Cleared
0
Denied
Cypris Medical has 2 FDA 510(k) cleared medical devices. Based in Chicago, US.
Latest FDA clearance: May 2024. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cypris Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cypris Medical
2 devices