510(k) · Cleared
ClearedBruno Vertical Platform Lift, Model VPL-3100
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Bruno Independent Living Aids, Inc. · ING Elevator, Wheelchair, Portable
Cleared on Jul 13, 2006 after a 42-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 3 later devices descend from it.
- Decided
- Jul 13, 2006
- Review
- 42 days
- Class
- Class II
- Product code
- ING
- Recalls
- None
- Predicates
- 0
3 later devices descend from it, 3 citing it directly.
- This deviceK061514 Bruno Vertical Platform Lift, Model VPL-3100Bruno Independent Living Aids, Inc. · 2006
- Descendant · cites it directly · 1 of its ownK091881 RPL/CPL Vertical Platform LiftsHarmar Summit, LLC · 2009
- Descendant · cites it directly · 0 of its ownK113065 RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC · 2012
- Descendant · cites it directly · 0 of its ownK073513 Merits E700 Porce LiftMerits Health Products Co., Ltd. · 2008
Most influential descendants
Showing 3 of 3 · See all- K091881RPL/CPL Vertical Platform LiftsHarmar Summit, LLC · 2009 · cites it directly1descendant
- K113065RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC · 2012 · cites it directly0descendants
- K073513Merits E700 Porce LiftMerits Health Products Co., Ltd. · 2008 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K061514 | Bruno Vertical Platform Lift, Model VPL-3100 | Bruno Independent Living Aids, Inc. | 2006 | — |
| +1 | K091881 | RPL/CPL Vertical Platform Lifts | Harmar Summit, LLC | 2009 | — |
| +1 | K113065 | RL, UL, SL, EL, and Epl Vertical Platform Lifts | Bella Elevator, LLC | 2012 | — |
| +1 | K073513 | Merits E700 Porce Lift | Merits Health Products Co., Ltd. | 2008 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2008 | 1 | 0 |
| 2009 | 1 | 0 |
| 2012 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in ING? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it? (3)
3 later devices cite it directly; ranked here by how many devices descend from each in turn.
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.
What does this lineage say?
- Of its descendants, K091881 (Harmar Summit, LLC, 2009) has gone furthest, with 1 descendant of its own.
How does its category compare?
All ING devicesING Elevator, Wheelchair, Portable: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · ING
1in 2012
2026 to Oct 25, outlined.
Median 510(k) review, days · ING
Too few ING 510(k)s in any year since 2007 to give a median.
Recalls per year · ING
3in 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · ING
4in 2024
MAUDE reports naming product code ING, 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 | 0 | — | 3 | 0 |
| 2008 | 1 | — | 0 | 0 |
| 2009 | 2 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 1 |
| 2011 | 1 | — | 0 | 0 |
| 2012 | 1 | — | 0 | 1 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 2 |
| 2018 | 0 | — | 0 | 7 |
| 2019 | 0 | — | 0 | 4 |
| 2020 | 0 | — | 0 | 7 |
| 2021 | 0 | — | 0 | 6 |
| 2022 | 0 | — | 0 | 3 |
| 2023 | 0 | — | 0 | 2 |
| 2024 | 0 | — | 0 | 4 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The VPL-3100 is intended to mechanically transport an individual with a mobility disability,
either in a wheelchair device or ambulatory, from one level to another in a private residence.
Indications for use as stated in the FDA 510(k) statement.
https://510kreport.com/device/K061514 · printed Nov 6, 2026
Cite this page
510(k) Report. “K061514: Bruno Vertical Platform Lift, Model VPL-3100.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K061514
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026