Finemedix Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250994ClearTip FNA and FNB TypesAugust 21, 2025
K242857ClearHemograsperMay 21, 2025
K242134ClearCap Distal AttachmentAugust 20, 2024
K231267ClearTipJune 30, 2023
K202616ClearCap Distal AttachmentFebruary 19, 2021
K200217ClearEndoclipOctober 5, 2020
K183021ClearEndoclipJune 28, 2019
K183289ClearGrasp SnareMarch 6, 2019
K181690Clear-Jet Injection CatheterDecember 21, 2018
K180363Clear-Tip EUS-FNANovember 1, 2018