Feeltech Co., Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Feeltech Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Gunsan-Si, KR.
Latest FDA clearance: Oct 2025. Active since 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Feeltech Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Feeltech Co., Ltd.
4 devices
Cleared
Oct 20, 2025
Miracu™ Polydioxanone (PDO) Suture and Needle (MONO)
General & Plastic Surgery
166d
Cleared
Oct 15, 2025
V-soft Line™ Barbed Surgical Suture (Various)
General & Plastic Surgery
273d
Cleared
May 31, 2023
FEELject LDV (Low dead volume) syringe
General Hospital
618d
Cleared
Nov 14, 2018
Miracu
General & Plastic Surgery
441d