Medical Device Manufacturer · KR , Gunsan-Si

Feeltech Co., Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2018

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

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), Albert Rego, PhD, Inc. and Plusglobal.

FDA 510(k) Regulatory Record - Feeltech Co., Ltd.

4 devices
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