# K070676: Korebalance (Kinesthetic Ability Trainer)

- Pathway: 510(k) (Special)
- Applicant: Sportkat, LLC
- Decided: Apr 18, 2007 after 37 days
- Product code: LXV (Apparatus, Vestibular Analysis)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K911795 (1991). 1 ancestor in all.
5 later devices descend from it; 2 cite 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)
- K911795: Kinesthetic Ability Trainer (K.a.T., Model 1000), Breg, Inc. (1991) Summary page 1.

## Most influential descendants
- K121590: Vestibular Analysis Apparatus (2012), 3 descendants of its own
- K183661: ClearEdge Balance System (2019), 0 descendants of its own
- K190735: EQ Balance (2019), 0 descendants of its own
- K173669: K-D Balance (2018), 0 descendants of its own
- K081602: Dizzyfix (2008), 0 descendants of its own

## Indications for use
The KorebalanceTM device is intended for use in balance therapy, only by health care professionals with experience in balance therapy. Patient suitability must be judged by the health professional on a case by case basis.

Source page: https://510kreport.com/device/K070676
Methodology: https://510kreport.com/methodology