Finemedix Co., Ltd. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Finemedix Co., Ltd. has 11 FDA 510(k) cleared gastroenterology & urology devices. Based in Daegu, KR.
Latest FDA clearance: Apr 2026. Active since 2018.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by LK Consulting Group USA, Inc., Withus Group, Inc. and KMC, Inc..
11 devices
Cleared
Apr 16, 2026
ClearTip TBNA Type
Anesthesiology
338d
Cleared
Aug 21, 2025
ClearTip FNA and FNB Types
Gastroenterology & Urology
142d
Cleared
May 21, 2025
ClearHemograsper
Gastroenterology & Urology
243d
Cleared
Aug 20, 2024
ClearCap Distal Attachment
Gastroenterology & Urology
29d
Cleared
Jun 30, 2023
ClearTip
Gastroenterology & Urology
59d
Cleared
Feb 19, 2021
ClearCap Distal Attachment
Gastroenterology & Urology
163d
Cleared
Oct 05, 2020
ClearEndoclip
Gastroenterology & Urology
251d
Cleared
Jun 28, 2019
ClearEndoclip
Gastroenterology & Urology
239d
Cleared
Mar 06, 2019
ClearGrasp Snare
Gastroenterology & Urology
100d
Cleared
Dec 21, 2018
Clear-Jet Injection Catheter
Gastroenterology & Urology
178d
Cleared
Nov 01, 2018
Clear-Tip EUS-FNA
Gastroenterology & Urology
265d