Cleared Traditional

Endomina EZFuse system

K252400 · Endo Tools Therapeutics S.A. · Gastroenterology & Urology
Feb 2026
Decision
197d
Days
Class 2
Risk

About This 510(k) Submission

K252400 is an FDA 510(k) clearance for the Endomina EZFuse system, a Endoscopic Tissue Approximation Device (Class II — Special Controls, product code OCW), submitted by Endo Tools Therapeutics S.A. (Gosselies, BE). The FDA issued a Cleared decision on February 13, 2026, 197 days after receiving the submission on July 31, 2025. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K252400 FDA.gov
FDA Decision Cleared SESE
Date Received July 31, 2025
Decision Date February 13, 2026
Days to Decision 197 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code OCW — Endoscopic Tissue Approximation Device
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Aid In Endoscopically Placing Sutures, Staples, Clips, And Other Fastening Tools Through Tissue.

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