FDA product code · Orthopedic
Stimulator, Invasive Bone Growth
2 FDA decisions since 1980. 2 recalls name this code, 2 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 LOE 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 · LOE
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · LOE
Too few LOE 510(k)s in any year since 2007 to give a median.
Recalls per year · LOE
2in 2018
Class I (2 since 2007) Class II/III not classified
Adverse event reports per year · LOE
7in 2025
MAUDE reports naming product code LOE, 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 | 2 |
| 2008 | 3 | — | 0 | 32 |
| 2009 | 0 | — | 0 | 3 |
| 2010 | 0 | — | 0 | 3 |
| 2011 | 1 | — | 0 | 7 |
| 2012 | 2 | — | 0 | 4 |
| 2013 | 4 | — | 0 | 3 |
| 2014 | 2 | — | 0 | 3 |
| 2015 | 4 | — | 0 | 6 |
| 2016 | 4 | — | 0 | 5 |
| 2017 | 4 | — | 0 | 5 |
| 2018 | 16 | — | 2 (2) | 8 |
| 2019 | 4 | — | 0 | 10 |
| 2020 | 0 | — | 0 | 5 |
| 2021 | 2 | — | 0 | 3 |
| 2022 | 4 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 2 |
| 2024 | 1 | — | 0 | 2 |
| 2025 | 0 | — | 0 | 7 |
| 2026 | 0 | — | 0 | — |
Planning a device in LOE? 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