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.
Regulatory submissions have been managed by Albert Rego PHD, Inc (D.B.A Rego Associates) and Plusglobal.
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