510(k) · Cleared
ClearedJourney Inclined Platform Lift and Supra Curved Incline Platform Lift
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Thyssenkrupp Ceteco Srl · ING Elevator, Wheelchair, Portable
Cleared on Oct 20, 2010 as substantially equivalent to K090856 (Thyssenkrupp Ceteco Srl, 2009) after an 86-day review. Its family tree reaches back 4 generations to 1989.
- Decided
- Oct 20, 2010
- Review
- 86 days
- Class
- Class II
- Product code
- ING
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K893544 (1989). No later device cites it as a predicate yet.
- Root · 4 generations backK893544 Handi Porch Elevator & Liberty Wheelchair LiftThe Cheney Co. · 1989
- 3 generations backK960276 Wheelchair ElevatorServices Industriels Savaria, Inc. · 1996
- 2 generations backK981486 Stair-LiftGaraventa (Canada), Ltd. · 1998
- 1 generation backK090856 Journey (or RPSP), Journey Cubic (or Supra or TP02)Thyssenkrupp Ceteco Srl · 2009
- This deviceK102088 Journey Inclined Platform Lift and Supra Curved Incline Platform LiftThyssenkrupp Ceteco Srl · 2010
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K893544 | Handi Porch Elevator & Liberty Wheelchair Lift | The Cheney Co. | 1989 | — |
| −3 | K960276 | Wheelchair Elevator | Services Industriels Savaria, Inc. | 1996 | — |
| −2 | K981486 | Stair-Lift | Garaventa (Canada), Ltd. | 1998 | — |
| −1 | K090856 | Journey (or RPSP), Journey Cubic (or Supra or TP02) | Thyssenkrupp Ceteco Srl | 2009 | — |
| 0 (this device) | K102088 | Journey Inclined Platform Lift and Supra Curved Incline Platform Lift | Thyssenkrupp Ceteco Srl | 2010 | — |
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 ING? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin 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 |
|---|---|---|---|
| * | K090856 | Journey (or RPSP), Journey Cubic (or Supra or TP02)Summary page 1…SUPRA" h Common Device Name: Inclined Platform Lift (IPL) Predicate device: ThyssenKrijpp Ceteco Inclined Platform Lift "Journey. K090856, Product description: The Thyssenkrupp Ceteco's JOURNEY and SUPRA are unenclosed… | 2009 |
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 21 years and passes through 4 companies; a new generation was cleared every 6.8 years on median.
- None of the 4 ancestors has a recall.
How does its category compare?
All ING devicesING Elevator, Wheelchair, Portable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.
FDA decisions per year · ING
1in 2012
2026 to Oct 25, outlined.
Median 510(k) review, days · ING
Too few ING 510(k)s in any year since 2007 to give a median.
Recalls per year · ING
3in 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · ING
4in 2024
MAUDE reports naming product code ING, 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 | 0 | — | 3 | 0 |
| 2008 | 1 | — | 0 | 0 |
| 2009 | 2 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 1 |
| 2011 | 1 | — | 0 | 0 |
| 2012 | 1 | — | 0 | 1 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 2 |
| 2018 | 0 | — | 0 | 7 |
| 2019 | 0 | — | 0 | 4 |
| 2020 | 0 | — | 0 | 7 |
| 2021 | 0 | — | 0 | 6 |
| 2022 | 0 | — | 0 | 3 |
| 2023 | 0 | — | 0 | 2 |
| 2024 | 0 | — | 0 | 4 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Inclined Platform Lifts "JOURNEY" and "SUPRA" are intended to mechanically transport one person in a wheelchair or in a fold-down seat up and down stairs in a private or public facility.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K102088 · printed Nov 6, 2026
Cite this page
510(k) Report. “K102088: Journey Inclined Platform Lift and Supra Curved Incline Platform Lift.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K102088
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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