Agnes Medical Co., Ltd.

Agnes Medical Co., Ltd. holds 7 FDA 510(k) medical device clearances, first cleared 2019, most recent 2025.

Top product codes for Agnes Medical Co., Ltd.

GEI — General, Plastic Surgery7 devices

Recent clearances by Agnes Medical Co., Ltd.

K250217 — AGNES UltraCode GEI·2025-09-03
K243713 — Single Use RF Surgical Electrode (Needle Type) (AN-B, AN-C, AN-E, AN-I, AN-S, AN-W3A, AN-F3A, AN-IL, AN-SL, AN-W3B, AN-F1A, AN-F3B, AN-B3A)Code GEI·2025-08-19
K242469 — RFMagik LiteCode GEI·2025-04-25
K230837 — PlazMagikCode GEI·2024-02-29
K223805 — AgnesCode GEI·2023-05-04
K203013 — AGNESCode GEI·2022-07-14
K192728 — AgnesCode GEI·2019-10-24

Data sourced from openFDA. This site is unofficial and independent of the FDA.