FDA product code · Cardiovascular
Artificial Heart
1 FDA decision since 2004. 4 recalls name this code, 1 of them Class I.
P030011
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly Download the data (CSV)
Twenty years of LOZ 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 · LOZ
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LOZ
Too few LOZ 510(k)s in any year since 2007 to give a median.
Recalls per year · LOZ
1in 2023
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · LOZ
47in 2025
MAUDE reports naming product code LOZ, 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 | 1 | — | 0 | 0 |
| 2008 | 1 | — | 1 | 0 |
| 2009 | 1 | — | 0 | 3 |
| 2010 | 2 | — | 0 | 2 |
| 2011 | 2 | — | 0 | 32 |
| 2012 | 5 | — | 0 | 92 |
| 2013 | 3 | — | 0 | 156 |
| 2014 | 7 | — | 0 | 325 |
| 2015 | 7 | — | 0 | 421 |
| 2016 | 10 | — | 1 (1) | 422 |
| 2017 | 11 | — | 0 | 291 |
| 2018 | 5 | — | 0 | 569 |
| 2019 | 8 | — | 0 | 379 |
| 2020 | 5 | — | 0 | 264 |
| 2021 | 0 | — | 0 | 241 |
| 2022 | 2 | — | 1 | 152 |
| 2023 | 6 | — | 1 | 167 |
| 2024 | 2 | — | 0 | 80 |
| 2025 | 3 | — | 0 | 47 |
| 2026 | 2 | — | 0 | — |
Planning a device in LOZ? 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