# K051684: Eyeport Vision Training System

- Pathway: 510(k) (Traditional)
- Applicant: Exercise Your Eyes, Inc.
- Decided: Mar 17, 2006 after 267 days
- Product code: NXR (Fixation, Vision Training, Binocular)
- Device class: 1
- Regulation: 21 CFR 886.1290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Gruss Electro Wand: named in the summary without a submission number
- (no number) Vis-Flex: named in the summary without a submission number

## Indications for use
The EYEPORT is indicated for the treatment of poor accommodative and vergence facility, convergence insufficiency and large accommodative lag (in non-presbyopic subjects).

Source page: https://510kreport.com/device/K051684
Methodology: https://510kreport.com/methodology