# K980952: Snore-Cure Anti-Snoring Appliance

- Pathway: 510(k) (Traditional)
- Applicant: ORTHO-TAIN, Inc.
- Decided: Jun 1, 1998 after 80 days
- Product code: LRK (Device, Anti-Snoring)
- 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
Longest line of descent: 1 generation back to K882303 (1989). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K882303: H&M Anti-Snoring Device, Hays & Meade, Inc. (1989) Summary page 2.

## Indications for use
The SNORE-CURE Anti-snoring Appliance is intended as an aid in the alleviation of snoring by repositioning the lower jaw slightly forward and open together with the tongue to expand the patient’s airway, thereby decreasing air turbulence.

Source page: https://510kreport.com/device/K980952
Methodology: https://510kreport.com/methodology