Entrigue Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MEDIENT MIDDLE TURBINATE IMPLANT, SINUS DILATION SYSTEM, ENTACT SEPTAL STAPLER, MODEL 610-00100
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Entrigue Surgical, Inc. General & Plastic Surgery ✕
1 devices