Finemedix Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Finemedix Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ClearTip TBNA Type, ClearTip FNA and FNB Types, ClearHemograsper
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 Withus Group, Inc., LK Consulting Group USA, Inc. and K-Biotech, Inc..
FDA 510(k) Regulatory Record - Finemedix Co., Ltd.
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