510(k) Report

510(k) · Cleared

Cleared

Wu's 3-Wheeled Neo Scooter, WT-T3D

K032488510(k) TraditionalCleared Dec 2, 2003112-day reviewClass II21 CFR 890.3800

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

Wu'S Tech Co., Ltd. · INI Vehicle, Motorized 3-Wheeled

Cleared on Dec 2, 2003 after a 112-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 31 later devices descend from it.

Decided
Dec 2, 2003
Review
112 days
Class
Class II
Product code
INI
Recalls
None
Predicates
0

31 later devices descend from it, 6 citing it directly.

Descendants, by year cleared 2006: 1 descendant cleared2004: 2 descendants cleared2009: 4 descendants cleared2007: 3 descendants cleared2005: 1 descendant cleared2010: 2 descendants cleared2015: 5 descendants cleared2008: 1 descendant cleared2022: 2 descendants cleared2014: 1 descendant cleared2019: 1 descendant cleared2023: 1 descendant cleared2024: 2 descendants cleared2026: 4 descendants cleared2025: 1 descendant cleared200020052010201520202025
  1. This deviceK032488 Wu's 3-Wheeled Neo Scooter, WT-T3DWu'S Tech Co., Ltd. · 2003
  2. Descendant · cites it directly · 25 of its ownK071007 Heartway Lightweight Power Mobility Scooter, S33Heartway Medical Products Co., Ltd. · 2007
  3. Descendant · 2 generations on · 12 of its ownK101142 Heartway Lightweight Power Mobility Scooter, S34Heartway Medical Products Co., Ltd. · 2010
  4. Descendant · 2 generations on · 11 of its ownK072104 Heartway Power Mobility Scooter, PF6Heartway Medical Products Co., Ltd. · 2007
  5. Descendant · 3 generations on · 9 of its ownK150987 HEARTWAY Power Mobility Scooter, BRIO S19Heartway Medical Products Co., Ltd. · 2015
  6. Descendant · 3 generations on · 6 of its ownK073044 Heartway Power Mobility Scooter, Model PT7Heartway Medical Products Co., Ltd. · 2007

Showing 5 of 31 descendants. See all descendants

Descendants cleared per year

2004: 22005: 12006: 12007: 32008: 12009: 42010: 22014: 12015: 52019: 12022: 22023: 12024: 22025: 12026: 4
2004high 5 (2015) · low 0 (2011)2026

Most influential descendants

Showing 5 of 31 · See all
  • K071007Heartway Lightweight Power Mobility Scooter, S33Heartway Medical Products Co., Ltd. · 2007 · cites it directly25descendants
  • K101142Heartway Lightweight Power Mobility Scooter, S34Heartway Medical Products Co., Ltd. · 2010 · 2 generations on12descendants
  • K072104Heartway Power Mobility Scooter, PF6Heartway Medical Products Co., Ltd. · 2007 · 2 generations on11descendants
  • K150987HEARTWAY Power Mobility Scooter, BRIO S19Heartway Medical Products Co., Ltd. · 2015 · 3 generations on9descendants
  • K073044Heartway Power Mobility Scooter, Model PT7Heartway Medical Products Co., Ltd. · 2007 · 3 generations on6descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K032488Wu's 3-Wheeled Neo Scooter, WT-T3DWu'S Tech Co., Ltd.2003—
+1K071007Heartway Lightweight Power Mobility Scooter, S33Heartway Medical Products Co., Ltd.2007—
+2K101142Heartway Lightweight Power Mobility Scooter, S34Heartway Medical Products Co., Ltd.2010—
+2K072104Heartway Power Mobility Scooter, PF6Heartway Medical Products Co., Ltd.2007—
+3K150987HEARTWAY Power Mobility Scooter, BRIO S19Heartway Medical Products Co., Ltd.2015—
+3K073044Heartway Power Mobility Scooter, Model PT7Heartway Medical Products Co., Ltd.2007—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200420
200510
200610
200730
200810
200940
201020
201410
201550
201910
202220
202310
202420
202510
202640
FIG. 1 — Lineage of K032488, 2003–2026Source: 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 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
Get a 510(k) Report

What was it cleared against?

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

What descends from it? (31)

See all 31

6 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K071007Heartway Lightweight Power Mobility Scooter, S33Heartway Medical Products Co., Ltd.200725
K091212Wu's 3 Wheeled Electrical Scooter, WT-T3HWu'S Tech Co., Ltd.20090
K062790Wu's 3-Wheeled Neo Scooter, Model WT-T3EWu'S Tech Co., Ltd.20060
K052673King I Powered Scooter, Model CTL-11King I Tech Corporation20050
K041187A&I Scooter, SC-301Well Success Biotech, Inc.20040
K040968Wu's 4-Wheeled Neo Scooter, Model WT-T4DWu'S Tech Co., Ltd.20040

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, K071007 (Heartway Medical Products Co., Ltd., 2007) has gone furthest, with 25 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—

What is it indicated for?

The device is intended for medical purposes to provide mobility to persons restricted to

a seated position.

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

Cite this page

510(k) Report. “K032488: Wu's 3-Wheeled Neo Scooter, WT-T3D.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K032488

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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