510(k) · Cleared
ClearedZippie & Quickie 2HP Wheelchair
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Motion Designs, Inc. · IOR Wheelchair, Mechanical
Cleared on Feb 8, 1989 after a 33-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 6 later devices descend from it.
- Decided
- Feb 8, 1989
- Review
- 33 days
- Class
- Class I
- Product code
- IOR
- Recalls
- None
- Predicates
- 0
6 later devices descend from it, 6 citing it directly.
- This deviceK890050 Zippie & Quickie 2HP WheelchairMotion Designs, Inc. · 1989
- Descendant · cites it directly · 0 of its ownK103073 Super Chair for Kids by OrionFuture Mobility Healthcare, Inc. · 2011
- Descendant · cites it directly · 0 of its ownK102031 Galaxy LiteFuture Mobility Healthcare, Inc. · 2010
- Descendant · cites it directly · 0 of its ownK072311 Tilite Aero XTisport, LLC · 2007 · Recalled
- Descendant · cites it directly · 0 of its ownK023606 Tilite YG and Tilite YgsTisport · 2002 · Recalled
- Descendant · cites it directly · 0 of its ownK990555 Tisport X and Tisport XCTisport · 1999
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K103073Super Chair for Kids by OrionFuture Mobility Healthcare, Inc. · 2011 · cites it directly0descendants
- K102031Galaxy LiteFuture Mobility Healthcare, Inc. · 2010 · cites it directly0descendants
- K072311Tilite Aero XTisport, LLC · 2007 · cites it directly0descendants
- K023606Tilite YG and Tilite YgsTisport · 2002 · cites it directly0descendants
- K990555Tisport X and Tisport XCTisport · 1999 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K890050 | Zippie & Quickie 2HP Wheelchair | Motion Designs, Inc. | 1989 | — |
| +1 | K103073 | Super Chair for Kids by Orion | Future Mobility Healthcare, Inc. | 2011 | — |
| +1 | K102031 | Galaxy Lite | Future Mobility Healthcare, Inc. | 2010 | — |
| +1 | K072311 | Tilite Aero X | Tisport, LLC | 2007 | 1 |
| +1 | K023606 | Tilite YG and Tilite Ygs | Tisport | 2002 | 1 |
| +1 | K990555 | Tisport X and Tisport XC | Tisport | 1999 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1999 | 2 | 0 |
| 2002 | 1 | 0 |
| 2007 | 1 | 0 |
| 2010 | 1 | 0 |
| 2011 | 1 | 0 |
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 IOR? 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 IOR device
- #1 K201461 Manual Wheelchair, Model A011score 20.0 · 3 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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? (6)
6 later devices cite it directly; ranked here by how many devices descend from each in turn.
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, K103073 (Future Mobility Healthcare, Inc., 2011) has gone furthest, with 0 descendants of its own.
How does its category compare?
All IOR devicesIOR Wheelchair, Mechanical: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · IOR
17so far in 2026, the most since 2007
2026 to Oct 25, outlined.
Median 510(k) review, days · IOR
91in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IOR
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IOR
135in 2025
MAUDE reports naming product code IOR, 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 | 5 | 38 | 1 | 36 |
| 2008 | 13 | 32 | 3 | 62 |
| 2009 | 4 | 43 | 2 | 54 |
| 2010 | 12 | 81 | 0 | 69 |
| 2011 | 6 | 58 | 6 | 232 |
| 2012 | 11 | 176 | 3 | 1,238 |
| 2013 | 7 | 233 | 3 | 4,674 |
| 2014 | 7 | 211 | 3 | 5,082 |
| 2015 | 3 | 104 | 0 | 4,472 |
| 2016 | 10 | 135 | 1 | 1,860 |
| 2017 | 7 | 209 | 0 | 49 |
| 2018 | 3 | 203 | 0 | 58 |
| 2019 | 6 | 160 | 0 | 53 |
| 2020 | 2 | — | 0 | 43 |
| 2021 | 2 | — | 1 | 59 |
| 2022 | 4 | 150 | 0 | 37 |
| 2023 | 9 | 61 | 0 | 165 |
| 2024 | 4 | 65 | 0 | 138 |
| 2025 | 7 | 91 | 0 | 135 |
| 2026 | 17 | 103 | 0 | — |
https://510kreport.com/device/K890050 · printed Nov 5, 2026
Cite this page
510(k) Report. “K890050: Zippie & Quickie 2HP Wheelchair.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K890050
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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