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Feeltech Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251414Miracu™ Polydioxanone (PDO) Suture and Needle (MONO)October 20, 2025
K250107V-soft Line™ Barbed Surgical Suture (Various)October 15, 2025
K213010FEELject LDV (Low dead volume) syringeMay 31, 2023
K172602MiracuNovember 14, 2018