PMA · Approved
ApprovedThe Disintegrator Plus Lance/Insulin Needle Destructon Device
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Redhawk Medical Products & Services, LLC · MTV Sharps Needle Destruction Device
Approved on Apr 18, 2002 through premarket approval, which rests on the device’s own clinical evidence after a 2-day review.
- Decided
- Apr 18, 2002
- Review
- 2 days
- Class
- Class II
- Product code
- MTV
- Recalls
- None
PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.
Sources: FDA PMA database (decision fields and supplements), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in MTV? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new MTV device
- #1 K202073 NeedleSmart Professional (NS Pro)score 1.1 · 1 generation · no Class I recall
Does it have a predicate?
PMA decisions do not claim a predicate device.
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
How does its category compare?
All MTV devicesMTV Sharps Needle Destruction Device: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · MTV
1in 2021
2026 to Oct 25, outlined.
Median 510(k) review, days · MTV
Too few MTV 510(k)s in any year since 2007 to give a median.
Recalls per year · MTV
No recall names MTV since 2007.
Adverse event reports per year · MTV
No MAUDE report names MTV since 2007.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 1 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/P010040/S001 · printed Nov 6, 2026
Cite this page
510(k) Report. “P010040/S001: The Disintegrator Plus Lance/Insulin Needle Destructon Device.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P010040/S001
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026