Agnes Medical Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250217AGNES UltraSeptember 3, 2025
K243713Single Use RF Surgical Electrode (Needle Type) (AN-B, AN-C, AN-E, AN-I, AN-S, AN-W3A, AN-F3A, AN-IL,August 19, 2025
K242469RFMagik LiteApril 25, 2025
K230837PlazMagikFebruary 29, 2024
K223805AgnesMay 4, 2023
K203013AGNESJuly 14, 2022
K192728AgnesOctober 24, 2019