# K151446: Recovr Rehabilitation System

- Pathway: 510(k) (Traditional)
- Applicant: Recovr,Inc
- Decided: Sep 18, 2015 after 112 days
- Product code: LXJ (Interactive Rehabilitation Exercise Devices)
- Device class: 2
- Regulation: 21 CFR 890.5360
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K890076 (1989). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130847: Jintronix Rehabilitation System (JRS), Jintronix, Inc. (2014) Summary page 4.

## Most influential descendants
- K172882: Uincare Home (2018), 0 descendants of its own

## Indications for use
The Recovr Rehabilitation System is software for use with the Microsoft Kinect motion tracking system that is indicated to support physical rehabilitation of adults in the clinic and at home via performance of therapist-assigned reach exercises for the upper extremities. Patient assessment, exercise guidance, and approval by the medical professional are required prior to use.

Source page: https://510kreport.com/device/K151446
Methodology: https://510kreport.com/methodology