510(k) Report

510(k) · Cleared

Cleared

Wheelchair Model STS

K071390510(k) AbbreviatedCleared Jul 20, 200763-day reviewClass II21 CFR 890.3900

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

Innovative Products, Inc. · IPL Wheelchair, Standup

Cleared on Jul 20, 2007 after a 63-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 1 later device descends from it.

Decided
Jul 20, 2007
Review
63 days
Class
Class II
Product code
IPL
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2020: 1 descendant cleared20052010201520202025
  1. This deviceK071390 Wheelchair Model STSInnovative Products, Inc. · 2007
  2. Descendant · cites it directly · 0 of its ownK190682 Explorer MiniPermobil AB · 2020

Most influential descendants

Showing 1 of 1 · See all
  • K190682Explorer MiniPermobil AB · 2020 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K071390Wheelchair Model STSInnovative Products, Inc.2007—
+1K190682Explorer MiniPermobil AB2020—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
FIG. 1 — Lineage of K071390, 2007–2020Source: 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 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 IPL? 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 IPL device

  1. #1 K203761 ParaMotionscore 3.3 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
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What was it cleared against?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K190682Explorer MiniPermobil AB20200

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, K190682 (Permobil AB, 2020) has gone furthest, with 0 descendants of its own.

How does its category compare?

All IPL devices

IPL Wheelchair, Standup: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · IPL

1in 2025

2007: 32008: 12009: 12010: 22013: 12015: 12018: 22019: 32020: 22022: 22025: 1
2007high 3 (2007) · low 0 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IPL

105in 2019

2007: 63 days median2019: 105 days median
2007high 105 (2019) · low 63 (2007)2026

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

Recalls per year · IPL

No recall names IPL since 2007.

Adverse event reports per year · IPL

5in 2025

2008: 12010: 12013: 32014: 12015: 32018: 12019: 12021: 42022: 32023: 92024: 62025: 5
2007high 9 (2023) · low 0 (2007)2025

MAUDE reports naming product code IPL, 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
200736300
20081—01
20091—00
20102—01
20110—00
20120—00
20131—03
20140—01
20151—03
20160—00
20170—00
20182—01
2019310501
20202—00
20210—04
20222—03
20230—09
20240—06
20251—05
20260—0—

What is it indicated for?

The intended use of the Model STS Pediatric powered wheelchair is to provide mobility to children and young adults, weighing up to 150 pounds, with the ability to place themselves in a sitting position in the wheelchair and have the capacity to operate a standard joystick hand control.

Indications for use as stated in the FDA 510(k) statement.

Cite this page

510(k) Report. “K071390: Wheelchair Model STS.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K071390

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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