510(k) · Cleared
ClearedYuGo System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Biogaming, Ltd. · LXJ Interactive Rehabilitation Exercise Devices
Cleared on Feb 5, 2016 as substantially equivalent to K130847 (Jintronix, Inc., 2014) after a 205-day review. Its family tree reaches back 4 generations to 1989.
- Decided
- Feb 5, 2016
- Review
- 205 days
- Class
- Class II
- Product code
- LXJ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K890076 (1989). 5 ancestors in all. No later device cites it as a predicate yet.
- Root · 4 generations backK890076 OrthotrakMotion Analysis Corp. · 1989
- 3 generations backK982425 Coda MPX30 Motion Analysis SystemPinsco Inc. Dba B & L Engineering · 1998
- 2 generations backK030714 Peak MotusPeak Performance Technologies, Inc. · 2003
- 1 generation backK130847 Jintronix Rehabilitation System (JRS)Jintronix, Inc. · 2014
- This deviceK151955 YuGo SystemBiogaming, Ltd. · 2016
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K890076 | Orthotrak | Motion Analysis Corp. | 1989 | — |
| −3 | K982425 | Coda MPX30 Motion Analysis System | Pinsco Inc. Dba B & L Engineering | 1998 | — |
| −2 | K030714 | Peak Motus | Peak Performance Technologies, Inc. | 2003 | — |
| −1 | K130847 | Jintronix Rehabilitation System (JRS) | Jintronix, Inc. | 2014 | — |
| 0 (this device) | K151955 | YuGo System | Biogaming, Ltd. | 2016 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2004 | 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? (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 |
|---|---|---|---|
| * | K130847 | Jintronix Rehabilitation System (JRS)Summary page 5…5-3 510(k) Premarket Notification 5.10 Predicate Device: Jintronix Rehabilitation System (“JRS”) (Jintronix Inc.), cleared under K130847; product code: LXJ (System, Optical Position/Movement Recording). 5.11 Intended Use / Indication for Use: A software system use… | 2014 |
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 27 years and passes through 5 companies; a new generation was cleared every 9.7 years on median.
- None of the 5 ancestors has a recall.
- 4 other devices also cite its predicate K130847.
How does its category compare?
All LXJ devicesLXJ Interactive Rehabilitation Exercise Devices: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, 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 lower and upper extremities 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 as stated in the FDA summary.
https://510kreport.com/device/K151955 · printed Nov 6, 2026
Cite this page
510(k) Report. “K151955: YuGo System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151955
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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