510(k) Report

510(k) · Cleared

Recalled · 2003

Models Lynx and Panther Motorized Scooters, Models Lynx SX-3, Lynx SX-3P, Lynx LX-3, Lynx LX-3, Panther LX-4

K010135510(k) TraditionalCleared Feb 16, 200130-day reviewClass II21 CFR 890.3800Recalls 1

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

Invacare Corp. · INI Vehicle, Motorized 3-Wheeled

Cleared on Feb 16, 2001 after a 30-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it. It has been recalled once.

Decided
Feb 16, 2001
Review
30 days
Class
Class II
Product code
INI
Recalls
1
Predicates
0

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

Descendants, by year cleared 2003: 1 descendant cleared200020052010201520202025
  1. This deviceK010135 Models Lynx and Panther Motorized Scooters, Models Lynx SX-3, Lynx…Invacare Corp. · 2001
  2. Descendant · cites it directly · 0 of its ownK030814 Invacare Adventure Series Scooters, Models Adventure SX-3 & LX-3Invacare Corp. · 2003

Most influential descendants

Showing 1 of 1 · See all
  • K030814Invacare Adventure Series Scooters, Models Adventure SX-3 & LX-3Invacare Corp. · 2003 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K010135Models Lynx and Panther Motorized Scooters, Models Lynx SX-3, Lynx SX-3P, Lynx…Invacare Corp.2001—
+1K030814Invacare Adventure Series Scooters, Models Adventure SX-3 & LX-3Invacare Corp.2003—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200310
FIG. 1 — Lineage of K010135, 2001–2003Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in INI? 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 INI device

  1. #1 K231428 Mobility Scooter (Models: W3431D)score 23.1 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K030814Invacare Adventure Series Scooters, Models Adventure SX-3 & LX-3Invacare Corp.20030

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Feb 10, 2003Not classifiedZ-0574-03OtherA short circuit within the charger harness may cause heat damage to the units with potential for fire.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K030814 (Invacare Corp., 2003) has gone furthest, with 0 descendants of its own.

How does its category compare?

All INI devices

INI Vehicle, Motorized 3-Wheeled: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · INI

21so far in 2026, the most since 2007

2007: 182008: 72009: 122010: 52011: 52012: 12013: 22014: 12015: 92016: 12017: 52018: 32019: 42020: 12021: 52022: 62023: 92024: 82025: 152026 (partial year): 21
2007high 21 (2026) · low 1 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · INI

111in 2025

2007: 29 days median2008: 28 days median2009: 41 days median2010: 46 days median2011: 130 days median2015: 202 days median2017: 191 days median2018: 266 days median2019: 298 days median2021: 575 days median2022: 159 days median2023: 123 days median2024: 137 days median2025: 111 days median2026 (partial year): 108 days median
2007high 575 (2021) · low 28 (2008)2026

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

Recalls per year · INI

1in 2013

2007: 22010: 32011: 32013: 1
2007high 3 (2010) · low 0 (2008)2026

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

Adverse event reports per year · INI

26in 2025

2007: 642008: 292009: 252010: 562011: 702012: 1722013: 4542014: 5672015: 1512016: 762017: 452018: 512019: 252020: 262021: 412022: 412023: 322024: 312025: 26
2007high 567 (2014) · low 25 (2009)2025

MAUDE reports naming product code INI, 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
20071829264
2008728029
20091241025
2010546356
20115130370
20121—0172
20132—1454
20141—0567
201592020151
20161—076
20175191045
20183266051
20194298025
20201—026
20215575041
20226159041
20239123032
20248137031
202515111026
2026211080—
Cite this page

510(k) Report. “K010135: Models Lynx and Panther Motorized Scooters, Models Lynx SX-3, Lynx SX-3P, Lynx LX-3, Lynx LX-3, Panther LX-4.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K010135

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026