FDA product code · Cardiovascular
Occluder, Patent Ductus, Arteriosus
2 FDA decisions since 2002. 5 recalls name this code, 0 of them Class I.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly Download the data (CSV)
Twenty years of MAE 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 · MAE
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MAE
Too few MAE 510(k)s in any year since 2007 to give a median.
Recalls per year · MAE
No recall names MAE since 2007.
Adverse event reports per year · MAE
178in 2025
MAUDE reports naming product code MAE, 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 | 13 | — | 0 | 2 |
| 2008 | 6 | — | 0 | 12 |
| 2009 | 9 | — | 0 | 15 |
| 2010 | 7 | — | 0 | 18 |
| 2011 | 7 | — | 0 | 18 |
| 2012 | 6 | — | 0 | 19 |
| 2013 | 5 | — | 0 | 16 |
| 2014 | 3 | — | 0 | 28 |
| 2015 | 2 | — | 0 | 24 |
| 2016 | 10 | — | 0 | 12 |
| 2017 | 3 | — | 0 | 23 |
| 2018 | 1 | — | 0 | 28 |
| 2019 | 6 | — | 0 | 53 |
| 2020 | 6 | — | 0 | 109 |
| 2021 | 1 | — | 0 | 76 |
| 2022 | 1 | — | 0 | 80 |
| 2023 | 1 | — | 0 | 127 |
| 2024 | 4 | — | 0 | 117 |
| 2025 | 1 | — | 0 | 178 |
| 2026 | 2 | — | 0 | — |
Planning a device in MAE? 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