SEW

Automated Endoscope Channel Cleaner

Product code
SEW
Device name
Automated Endoscope Channel Cleaner
Device class
Class 2
21 CFR
21 CFR 880.6994
Medical specialty
General Hospital
Marketing pathway
510(K)
510(k) clearances (last 3 years)
2
Summaries archived here
1 (direct download)
510(k) clearances (all years, FDA)
2 (all years; only the last 3 years are listed here)

FDA classification definition

An automated endoscope channel cleaner is a device intended to replace all or a portion of manual cleaning of internal passages and ports of compatible reusable flexible endoscopes. Cleaning is conducted using an agent that exerts physical force (e.g., friction) on single or multiple channels of compatible endoscopes for removal of soil. This device type is not intended to provide or replace high-level disinfection or sterilization.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (2)

Last three years. Most recent: 2026-03-05.

NumberDecision dateApplicantDevice nameSummary
K2532672026-03-05Nanosonics LimitedCORIS SystemPDF
DEN2400182025-03-19Nanosonics LimitedCORIS System

1 summaries are archived here for direct download.

Official FDA classification page: SEW
Classification and pathway per current FDA publications. Data from openFDA (CC0).