Gyrus Ent LLC - FDA 510(k) Cleared Devices
Recent clearances: RETROX TITANIUM TUBE SYSTEM FOR THE RETROX TRANSCUTANEOUS AIR CONDUCTION HEARING AID SYSTEM, DIEGO RF POWERED DISSECTOR AND DRILL SYSTEM CONSOLE, HEMOSTATIX, MODEL 2400Z THERMAL SCALPEL SYSTEM
28
Total
28
Cleared
0
Denied
FDA 510(k) Regulatory Record - Gyrus Ent LLC General Hospital ✕
1 devices