Coloplast Manufacturing Us, LLC - FDA 510(k) Cleared Devices
Recent clearances: SELF CATH CATHETER, DIGITEX SUTURE DELIVERY SYSTEM, MODEL 52025, DIGITEX SUTURE CARTRIDGE (SIZE O), MODEL 52026, DIGITEX SUTURE CARTRIDGE, VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEM
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Coloplast Manufacturing Us, LLC General & Plastic Surgery ✕
1 devices