Feeltech Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Miracu™ Polydioxanone (PDO) Suture and Needle (MONO), V-soft Line™ Barbed Surgical Suture (Various), FEELject LDV (Low dead volume) syringe
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Feeltech Co., Ltd. General Hospital ✕
1 devices