# LXJ: Interactive Rehabilitation Exercise Devices

- Device class: 2; regulation: 21 CFR 890.5360; FDA's rule: 510(k) required
- FDA decisions: 27
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 1998: 1
- 2003: 1
- 2004: 1
- 2009: 1
- 2014: 2
- 2015: 3
- 2016: 1
- 2017: 2
- 2018: 3
- 2019: 3

## Most-cited predicates
- K130847: Jintronix Rehabilitation System (JRS) (2014), cited by 5
- K030714: Peak Motus (2003), cited by 4
- K033514: Coda CX1 Motion Analysis System (2004), cited by 3
- K923033: The Tracker (1993), cited by 2
- K982425: Coda MPX30 Motion Analysis System (1998), cited by 2
- K131660: Smart (Smart-D, Smart-DX) (2014), cited by 1
- K151446: Recovr Rehabilitation System (2015), cited by 1
- K811172: VICON (1981), cited by 1
- K890076: Orthotrak (1989), cited by 1
- K162748: MindMotionPRO (2017), cited by 1

Source page: https://510kreport.com/product-code/LXJ
Data by year (CSV): https://510kreport.com/product-code/LXJ.csv