FDA product code · Gastroenterology and urology
Device, Incontinence, Mechanical/Hydraulic
2 FDA decisions since 2001. 4 recalls name this code, 0 of them Class I.
PMA to be filed by 12/26/00 (65 FR 57731 (9/26/00))
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly Download the data (CSV)
Twenty years of EZY 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 · EZY
6in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · EZY
Too few EZY 510(k)s in any year since 2007 to give a median.
Recalls per year · EZY
2in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · EZY
2,066in 2025
MAUDE reports naming product code EZY, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 6 | — | 0 | 7 |
| 2008 | 6 | — | 0 | 2 |
| 2009 | 7 | — | 0 | 14 |
| 2010 | 6 | — | 0 | 25 |
| 2011 | 4 | — | 1 | 26 |
| 2012 | 8 | — | 0 | 23 |
| 2013 | 2 | — | 0 | 22 |
| 2014 | 4 | — | 0 | 9 |
| 2015 | 9 | — | 0 | 13 |
| 2016 | 14 | — | 0 | 6 |
| 2017 | 12 | — | 0 | 9 |
| 2018 | 12 | — | 0 | 873 |
| 2019 | 10 | — | 0 | 2,753 |
| 2020 | 10 | — | 0 | 1,743 |
| 2021 | 3 | — | 1 | 1,697 |
| 2022 | 6 | — | 0 | 1,553 |
| 2023 | 4 | — | 0 | 1,778 |
| 2024 | 3 | — | 2 | 2,110 |
| 2025 | 6 | — | 0 | 2,066 |
| 2026 | 4 | — | 0 | — |
Planning a device in EZY? 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