510(k) · Cleared
ClearedGenesis Vertical Platform Lift
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Garaventa Accessibility · ING Elevator, Wheelchair, Portable
Cleared on Jan 7, 2004 as substantially equivalent to K960739 (Barnes,Richardson & Colburn, 1996) after a 65-day review. Its family tree reaches back 2 generations to 1994. 1 later device descends from it.
- Decided
- Jan 7, 2004
- Review
- 65 days
- Class
- Class II
- Product code
- ING
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K934553 (1994). 1 later device descends from it, 1 citing it directly.
- Root · 2 generations backK934553 Wheel-O-VatorThe National Wheel-O-Vator Co., Inc. · 1994
- 1 generation backK960739 V-1504 Vertical Platform LiftBarnes,Richardson & Colburn · 1996
- This deviceK033469 Genesis Vertical Platform LiftGaraventa Accessibility · 2004
- Descendant · cites it directly · 0 of its ownK113065 RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC · 2012
Most influential descendants
Showing 1 of 1 · See all- K113065RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC · 2012 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K934553 | Wheel-O-Vator | The National Wheel-O-Vator Co., Inc. | 1994 | — |
| −1 | K960739 | V-1504 Vertical Platform Lift | Barnes,Richardson & Colburn | 1996 | — |
| 0 (this device) | K033469 | Genesis Vertical Platform Lift | Garaventa Accessibility | 2004 | — |
| +1 | K113065 | RL, UL, SL, EL, and Epl Vertical Platform Lifts | Bella Elevator, LLC | 2012 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and 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? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K960739 | V-1504 Vertical Platform LiftSummary page 1…ift 3. Summary Common Device Name: Elevator, Wheolchair Trade Name: Genesis Verti al Platform Lift Predicate Device: V-1504 Vertic;: l Platform Lift (K960739) as manufactured by Services Industriels Savaria Inc. See the attac[ ed product liter… | 1996 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K113065 | RL, UL, SL, EL, and Epl Vertical Platform Lifts | 2012 | 0 |
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?
- The line of descent spans 10 years and passes through 3 companies; a new generation was cleared every 7.8 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K113065 (Bella Elevator, LLC, 2012) has gone furthest, with 0 descendants of its own.
- 2 other devices also cite its predicate K960739.
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 Genesis Vertical Platform Lift is intended to mechanically transport persons with a mobility disability, either in a wheelchair or ambulatory, up and down between levels of a residential or public facility.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K033469 · printed Nov 4, 2026
Cite this page
510(k) Report. “K033469: Genesis Vertical Platform Lift.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K033469
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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