FDA product code · Physical medicine

Elevator, Wheelchair, Portable

Name: FDA decisions, review times, recalls and adverse event reports for product code ING
Creator: 510(k) Report

INGClass II21 CFR 890.3930510(k) required29 decisions since 19853 recalls

29 FDA decisions since 1985. 3 recalls name this code, 0 of them Class I. The most-cited predicate is K960739, named by 3 later devices.

A motorized lift device that is not permanently mounted in one location and that is intended for medical purposes to provide a means to move a person with impaired mobility, with or without a wheelchair, from one level to another (e.g., portable platform lifts, attendant-operated stair climbing devices for wheelchairs).

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

FIG. A — Illustration, physical medicine panel

Twenty years of ING 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 · 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	—

FIG. 1 — ING by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in ING? 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

Related product codes

Other codes under 21 CFR 890.3930.

PCE Permanently Mounted Wheelchair Platform Lift

Elevator, Wheelchair, Portable

Which predicates do ING devices cite most?

Which ING devices have the deepest lineage?

What has FDA decided in ING lately?

What has been recalled in ING lately?

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