510(k) · Cleared
ClearedElevation
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Pdg Product Design Group, Inc. · IOR Wheelchair, Mechanical
Cleared on Oct 16, 2014 as substantially equivalent to K110985 (Icon Wheelchairs, Inc., 2011) after a 283-day review. Its family tree reaches back 6 generations to 1992.
- Decided
- Oct 16, 2014
- Review
- 283 days
- Class
- Class I
- Product code
- IOR
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 6 generations to K922535 (1992). 7 ancestors in all. No later device cites it as a predicate yet.
- Root · 6 generations backK922535 The TerminatorTop End Wheelchair Sports, Inc. · 1992
- 5 generations backK990157 Model Top End Terminator SS Manual WheelchairInvacare Corp. · 1999
- 4 generations backK012167 Model Top End Terminator Titanium Manual WheelchairInvacare Corp. · 2001
- 3 generations backK051369 Syryker Sorano WheelchairStryker Canada · 2005
- 2 generations backK082970 Marvel Wheelchair, Model EDCAL01Rogue Wheels, Inc. · 2008
- 1 generation backK110985 Icon Adult ManualIcon Wheelchairs, Inc. · 2011
- This deviceK140023 ElevationPdg Product Design Group, Inc. · 2014
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K922535 | The Terminator | Top End Wheelchair Sports, Inc. | 1992 | — |
| −5 | K990157 | Model Top End Terminator SS Manual Wheelchair | Invacare Corp. | 1999 | — |
| −4 | K012167 | Model Top End Terminator Titanium Manual Wheelchair | Invacare Corp. | 2001 | — |
| −3 | K051369 | Syryker Sorano Wheelchair | Stryker Canada | 2005 | — |
| −2 | K082970 | Marvel Wheelchair, Model EDCAL01 | Rogue Wheels, Inc. | 2008 | — |
| −1 | K110985 | Icon Adult Manual | Icon Wheelchairs, Inc. | 2011 | — |
| 0 (this device) | K140023 | Elevation | Pdg Product Design Group, Inc. | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
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 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? (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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K110985 | Icon Adult ManualSummary page 5…de IOR Predicate Device The Elevation Manual Wheelchair is substantially equivalent to the Icon Wheelchairs ICON Adult Manual Wheelchair (K110985) Page 1 of 5 K140023 510(k)… | 2011 |
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?
- The line of descent spans 22 years and passes through 6 companies; a new generation was cleared every 3.5 years on median.
- None of the 7 ancestors has a recall.
How does its category compare?
All IOR devicesIOR Wheelchair, Mechanical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
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 | — |
What is it indicated for?
The Elevation Manual Wheelchair is intended to provide mobility to persons limited to a seated position.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K140023 · printed Nov 6, 2026
Cite this page
510(k) Report. “K140023: Elevation.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K140023
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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