# K171529: Snorer's Friend

- Pathway: 510(k) (Abbreviated)
- Applicant: Scope Healthcare Technologies Pty, Ltd.
- Decided: Jan 2, 2018 after 222 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: 4 generations back to K882303 (1989). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061688: Anti-Snoring / Sleep Apnea Device, Tomed Dr. Toussaint GmbH (2006) Summary page 4.

## Indications for use
Snorer’s Friend is an intra-oral mandibular advancement device used during sleep to reduce snoring and treat mild to moderate Obstructive Sleep Apnea (OSA) in adults.

Source page: https://510kreport.com/device/K171529
Methodology: https://510kreport.com/methodology