ClearanceBrief
Company ยท KR

Finemedix Co., Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2026. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FCGBiopsy Needle3
OCXEndoscopic Irrigation/Suction System2
PKLHemostatic Metal Clip For The Gi Tract2
FBKEndoscopic Injection Needle, Gastroenterology-Urology1
FDISnare, Flexible1
KGEForceps, Biopsy, Electric1
KTIBronchoscope Accessory1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 16, 2026K251478ClearTip TBNA Type
Finemedix Co., Ltd., KR
KTI
Aug 21, 2025K250994ClearTip FNA and FNB Types
Finemedix Co., Ltd., KR
FCG
May 21, 2025K242857ClearHemograsper
Finemedix Co., Ltd., KR
KGE
Aug 20, 2024K242134ClearCap Distal Attachment
Finemedix Co., Ltd., KR
OCX
Jun 30, 2023K231267ClearTip
Finemedix Co., Ltd., KR
FCG
Feb 19, 2021K202616ClearCap Distal Attachment
Finemedix Co., Ltd., KR
OCX
Oct 5, 2020K200217ClearEndoclip
Finemedix Co., Ltd., KR
PKL
Jun 28, 2019K183021ClearEndoclip
Finemedix Co., Ltd., KR
PKL
Mar 6, 2019K183289ClearGrasp Snare
Finemedix Co., Ltd., KR
FDI
Dec 21, 2018K181690Clear-Jet Injection Catheter
Finemedix Co., Ltd., KR
FBK
Nov 1, 2018K180363Clear-Tip EUS-FNA
Finemedix Co., Ltd., KR
FCG

Latest recalls

DateFirm and productCodeLinked 510(k)
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