510(k) Report

FDA product code · Dental

Handpiece, Air-Powered, Root Canal Irrigation

NYLClass I21 CFR 872.4200510(k) required5 decisions since 20060 recalls

5 FDA decisions since 2006. 510(k) reviews decided 2021–2025 took a median of 181 days (half between 181 and 181). No recall names this code. The most-cited predicate is K140685, named by 2 later devices.

To clean the root canal prior to filling and used for root canal irrigation.

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

FIG. A — Illustration, dental panel

Twenty years of NYL at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · NYL

1in 2021

2010: 12014: 12016: 12021: 1
2007high 1 (2010) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NYL

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

Recalls per year · NYL

No recall names NYL since 2007.

Adverse event reports per year · NYL

No MAUDE report names NYL since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20101—00
20110—00
20120—00
20130—00
20141—00
20150—00
20161—00
20170—00
20180—00
20190—00
20200—00
20211—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — NYL by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NYL? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 872.4200.