510(k) Report

510(k) · Cleared

Cleared

Stairfriend Curved Stairway Chairlift

K023852510(k) TraditionalCleared Mar 4, 2003105-day reviewClass II21 CFR 890.5150

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

Services Industriels Savaria, Inc. · ILK Transport, Patient, Powered

Cleared on Mar 4, 2003 as substantially equivalent to K970927 (Bruno Independent Living Aids, Inc., 1997) after a 105-day review. Its family tree reaches back 1 generation to 1997.

Decided
Mar 4, 2003
Review
105 days
Class
Class II
Product code
ILK
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K970927 (1997). No later device cites it as a predicate yet.

K970927 · Bruno Electra-Ride Iii Stairway Elevator System · Bruno Independent Living Aids, Inc. · 199719961998200020022004
  1. Root · 1 generation backK970927 Bruno Electra-Ride Iii Stairway Elevator SystemBruno Independent Living Aids, Inc. · 1997
  2. This deviceK023852 Stairfriend Curved Stairway ChairliftServices Industriels Savaria, Inc. · 2003
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K970927Bruno Electra-Ride Iii Stairway Elevator SystemBruno Independent Living Aids, Inc.1997—
0 (this device)K023852Stairfriend Curved Stairway ChairliftServices Industriels Savaria, Inc.2003—
FIG. 1 — Lineage of K023852, 1997–2003Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 ILK? 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 ILK device

  1. #1 K222818 Xpedition ™ Powered Stair Chair (625700000000)score 5.3 · 3 generations · no Class I recall
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K970927Bruno Electra-Ride Iii Stairway Elevator System
Summary page 1
…te Prepared: November 1,2002 Subject Device: "Stairfriend" Curved Stairway Chairlift XO X A ? x Predicate Device: .Bruno Electra-Ride I11 ( 5 1O(k) number K970927) Subject Product Description: The Stairfriend is a curved stairway chairlift designed to carry a rated load…
Bruno Independent Living Aids, Inc.1997—

Also cleared against K970927: 1 other 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.

What does this lineage say?

  • Its one ancestor has no recall.
  • 1 other device also cites its predicate K970927.

How does its category compare?

All ILK devices

ILK Transport, Patient, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · ILK

1in 2024

2008: 12009: 12010: 22011: 12012: 32014: 12023: 12024: 1
2007high 3 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ILK

150in 2012

2012: 150 days median
2007high 150 (2012)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · ILK

1in 2012

2012: 1
2007high 1 (2012) · low 0 (2007)2026

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

Adverse event reports per year · ILK

32in 2025

2007: 12008: 42010: 12011: 12012: 42013: 42014: 22015: 22023: 52024: 182025: 32
2007high 32 (2025) · low 0 (2009)2025

MAUDE reports naming product code ILK, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—01
20081—04
20091—00
20102—01
20111—01
2012315014
20130—04
20141—02
20150—02
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20231—05
20241—018
20250—032
20260—0—

What is it indicated for?

The product will be used by patients to assist in navigating a specific set of stairs. This is a self-contained product that is mounted to the tread of a staircase. A trained dealer will install the unit, test it and teach the end user how to operate it. The typical user is someone who has limited function of their knees, hips or ankles and/or has trouble bending these joints. Other users include rehabilitated stroke victims, those inflicted with MS…

Read the full statement (163 words)

The product will be used by patients to assist in navigating a specific set of stairs. This is a self-contained product that is mounted to the tread of a staircase. A trained dealer will install the unit, test it and teach the end user how to operate it. The typical user is someone who has limited function of their knees, hips or ankles and/or has trouble bending these joints. Other users include rehabilitated stroke victims, those inflicted with MS, arthritis, heart disease, and those who cannot handle the exertion of walking up and down stairs. Doctors or physical therapists may recommend the unit for those who are recuperating, but a large number of users acquire a stairway elevator just because it eases the burden of climbing stairs, improving their quality of life. For those who are wheelchair bound, it requires that they be able to transfer and is usually an option only if the physical limitations of the residence prohibits a vertical elevator.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K023852: Stairfriend Curved Stairway Chairlift.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K023852

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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