Feeltech Co., Ltd. FDA Approvals

0 new drug approvals and 3 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Miracu Polydioxanone (PDO) Suture and Needle (MONO)510(k)Oct 20, 2025General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Oct 20, 2025
V-soft Line Barbed Surgical Suture (Various)510(k)Oct 15, 2025General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Oct 15, 2025
FEELject LDV (Low dead volume) syringe510(k)May 31, 2023General Hospital	General Hospital	510(k)Substantially Equivalent (Traditional)	May 31, 2023