510(k) Report

De Novo · Granted

Granted

CORIS System

DEN240018De NovoGranted Mar 19, 2025322-day reviewClass II21 CFR 880.6994

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Nanosonics Limited · SEW Automated Endoscope Channel Cleaner

Granted on Mar 19, 2025 as a new device type through De Novo after a 322-day review. 1 later device descends from it.

Decided
Mar 19, 2025
Review
322 days
Class
Class II
Product code
SEW
Recalls
None

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2026: 1 descendant cleared2026
  1. This deviceDEN240018 CORIS SystemNanosonics Limited · 2025
  2. Descendant · cites it directly · 0 of its ownK253267 CORIS SystemNanosonics Limited · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K253267CORIS SystemNanosonics Limited · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)DEN240018CORIS SystemNanosonics Limited2025—
+1K253267CORIS SystemNanosonics Limited2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of DEN240018, 2025–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA De Novo database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in SEW? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new SEW device

  1. #1 K253267 CORIS Systemscore 11.0 · 1 generation · no Class I recall
Get a 510(k) Report

Does it have a predicate?

De Novo decisions do not claim a predicate device.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K253267CORIS SystemNanosonics Limited20260

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K253267 (Nanosonics Limited, 2026) has gone furthest, with 0 descendants of its own.

How does its category compare?

All SEW devices

SEW Automated Endoscope Channel Cleaner: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · SEW

1in 2025

2025: 12026 (partial year): 1
2007high 1 (2025) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · SEW

Too few SEW 510(k)s in any year since 2007 to give a median.

Recalls per year · SEW

No recall names SEW since 2007.

Adverse event reports per year · SEW

No MAUDE report names SEW since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20251—00
20261—0—

What is it indicated for?

The Nanosonics CORIS System is indicated for cleaning of the channels of the Olympus EVIS EXERA III CF-HQ190L colonovideoscope.

The CORIS System is suitable for use in healthcare facilities by trained healthcare workers.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “DEN240018: CORIS System.” Lineage record from FDA De Novo data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/DEN240018

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026