510(k) · Cleared

Cleared

RPL/CPL Vertical Platform Lifts

K091881510(k) TraditionalCleared Jul 1, 20097-day reviewClass II21 CFR 890.3930

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Harmar Summit, LLC · ING Elevator, Wheelchair, Portable

Cleared on Jul 1, 2009 as substantially equivalent to K061514 (Bruno Independent Living Aids, Inc., 2006) after a 7-day review. Its family tree reaches back 1 generation to 2006. 1 later device descends from it.

Decided: Jul 1, 2009
Review: 7 days
Class: Class II
Product code: ING
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K061514 (2006). 1 later device descends from it, 1 citing it directly.

By dateBy generation

Root · 1 generation backK061514 Bruno Vertical Platform Lift, Model VPL-3100Bruno Independent Living Aids, Inc. · 2006
This deviceK091881 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

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
−1	K061514	Bruno Vertical Platform Lift, Model VPL-3100	Bruno Independent Living Aids, Inc.	2006	—
0 (this device)	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	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2012	1	0

FIG. 1 — Lineage of K091881, 2006–2012Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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

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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	Applicant	Decided	Recalls
*	K061514	Bruno Vertical Platform Lift, Model VPL-3100	Bruno Independent Living Aids, Inc.	2006	—

Also cleared against K061514: 2 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K113065	RL, UL, SL, EL, and Epl Vertical Platform Lifts	Bella Elevator, LLC	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?

Its one ancestor has no 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 K061514.

How does its category compare?

All ING devices

ING Elevator, Wheelchair, Portable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · ING

1in 2012

2007high 2 (2009) · low 0 (2007)2026

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

2007high 3 (2007) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · ING

4in 2024

2007high 7 (2018) · low 0 (2007)2025

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 intended use of the Hanmar Summit RPL/CPL Vertical Platform Lifts is to 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/K091881 · printed Nov 6, 2026

Cite this page

510(k) Report. “K091881: RPL/CPL Vertical Platform Lifts.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K091881

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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