510(k) · Cleared
ClearedJintronix Rehabilitation System (JRS)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Jintronix, Inc. · LXJ Interactive Rehabilitation Exercise Devices
Cleared on Feb 28, 2014 as substantially equivalent to K030714 (Peak Performance Technologies, Inc., 2003) and 1 other predicate after a 339-day review. Its family tree reaches back 3 generations to 1989. 6 later devices descend from it.
- Decided
- Feb 28, 2014
- Review
- 339 days
- Class
- Class II
- Product code
- LXJ
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 3 generations to K890076 (1989). 4 ancestors in all. 6 later devices descend from it, 5 citing it directly.
- Root · 3 generations backK890076 OrthotrakMotion Analysis Corp. · 1989
- 2 generations backK982425 Coda MPX30 Motion Analysis SystemPinsco Inc. Dba B & L Engineering · 1998
- 1 generation backK030714 Peak MotusPeak Performance Technologies, Inc. · 2003
- This deviceK130847 Jintronix Rehabilitation System (JRS)Jintronix, Inc. · 2014
- Descendant · cites it directly · 1 of its ownK151446 Recovr Rehabilitation SystemRecovr,Inc · 2015
- Descendant · 2 generations on · 0 of its ownK172882 Uincare HomeUincare Corp. · 2018
- Descendant · cites it directly · 0 of its ownK163245 Virtual Occupational Therapy Application (VOTA)Barron Associates, Inc. · 2017
- Descendant · cites it directly · 0 of its ownK151955 YuGo SystemBiogaming, Ltd. · 2016
- Descendant · cites it directly · 0 of its ownK150462 VeraReflexion Health, Inc. · 2015
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K151446Recovr Rehabilitation SystemRecovr,Inc · 2015 · cites it directly1descendant
- K172882Uincare HomeUincare Corp. · 2018 · 2 generations on0descendants
- K163245Virtual Occupational Therapy Application (VOTA)Barron Associates, Inc. · 2017 · cites it directly0descendants
- K151955YuGo SystemBiogaming, Ltd. · 2016 · cites it directly0descendants
- K150462VeraReflexion Health, Inc. · 2015 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K890076 | Orthotrak | Motion Analysis Corp. | 1989 | — |
| −2 | K982425 | Coda MPX30 Motion Analysis System | Pinsco Inc. Dba B & L Engineering | 1998 | — |
| −1 | K030714 | Peak Motus | Peak Performance Technologies, Inc. | 2003 | — |
| 0 (this device) | K130847 | Jintronix Rehabilitation System (JRS) | Jintronix, Inc. | 2014 | — |
| +1 | K151446 | Recovr Rehabilitation System | Recovr,Inc | 2015 | — |
| +2 | K172882 | Uincare Home | Uincare Corp. | 2018 | — |
| +1 | K163245 | Virtual Occupational Therapy Application (VOTA) | Barron Associates, Inc. | 2017 | — |
| +1 | K151955 | YuGo System | Biogaming, Ltd. | 2016 | — |
| +1 | K150462 | Vera | Reflexion Health, Inc. | 2015 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2004 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2015 | 3 | 0 |
| 2016 | 1 | 0 |
| 2017 | 1 | 0 |
| 2018 | 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 LXJ? 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? (2)
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 |
|---|---|---|---|
| * | K030714 | Peak MotusSummary page 2…unknown 51 0(k) Su bmitter I Peak Performance Technologies Charnwood Dynamics Limited Holder Inc. 510(k) Number K030714 K033514 Device Panel _ Physical Medicine Physical Medicine Product Code… | 2003 |
| * | K033514 | Coda CX1 Motion Analysis SystemSummary page 2…mitter I Peak Performance Technologies Charnwood Dynamics Limited Holder Inc. 510(k) Number K030714 K033514 Device Panel _ Physical Medicine Physical Medicine Product Code LXJ… | 2004 |
What descends from it? (6)
5 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?
- The line of descent spans 25 years and passes through 4 companies; a new generation was cleared every 9.7 years on median.
- None of the 4 ancestors has a recall.
- Of its descendants, K151446 (Recovr,Inc, 2015) has gone furthest, with 1 descendant of its own.
- 3 other devices also cite its predicate K030714.
How does its category compare?
All LXJ devicesLXJ Interactive Rehabilitation Exercise Devices: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · LXJ
3in 2019
2026 to Oct 25, outlined.
Median 510(k) review, days · LXJ
224in 2019
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LXJ
No recall names LXJ since 2007.
Adverse event reports per year · LXJ
1in 2018
MAUDE reports naming product code LXJ, 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 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 2 | — | 0 | 0 |
| 2015 | 3 | 182 | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 2 | — | 0 | 0 |
| 2018 | 3 | 231 | 0 | 1 |
| 2019 | 3 | 224 | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
A software system used with the Microsoft Kinect intended to be used to support the physical rehabilitation of adults in the clinic/ at home. The system includes rehabilitation exercises for the upper extremity and trunk with audio-visual feedback & graphic movement representations for patients as well as remotely accessible patient performance metrics for the medical professional. Patient assessment, exercise guidance and approval by the medical professional is required prior to use.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K130847 · printed Nov 5, 2026
Cite this page
510(k) Report. “K130847: Jintronix Rehabilitation System (JRS).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K130847
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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