# K971818: Snorex

- Pathway: 510(k) (Traditional)
- Applicant: Snorex (Nz), Ltd.
- Decided: Dec 18, 1997 after 216 days
- Product code: LQZ (Device, Jaw Repositioning)
- Device class: 2
- Regulation: 21 CFR 872.5570
- 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) The Silencer Appliance: named in the summary without a submission number

## Indications for use
The use of the SNOREX device is indicated for anyone who snores, has a desire to alleviate or eliminate snoring, and has sufficient natural upper and lower teeth to hold the appliance in place while sleeping.

Source page: https://510kreport.com/device/K971818
Methodology: https://510kreport.com/methodology