# K991449: Snore-Aid Plus

- Pathway: 510(k) (Traditional)
- Applicant: Dental Imagineers, LLC
- Decided: Jul 22, 1999 after 87 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). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K955336: Snorefree, Scott Feldman Dds & Norman Shapiro Dds (1996) Summary page 1.
- K882303: H&M Anti-Snoring Device, Hays & Meade, Inc. (1989) Summary page 1.

## Most influential descendants
- K022284: Snore-Aid Max (2002), 0 descendants of its own

## Indications for use
Snore-Aid®plus is prescribed for the patient by the healthcare professional. A. Snore-Aid®plus is indicated for use in patients with primary snoring or snoring and mild obstructive sleep apnea (OSA) where mandibular-advancement and positioning of the tongue can increase pharyngeal air space. B. Snore-Aid®plus is indicated to prevent symptoms of nocturnal parafunctional jaw activity in patients undergoing treatment for snoring and OSA by mandibular advancement and tongue positioning.

Source page: https://510kreport.com/device/K991449
Methodology: https://510kreport.com/methodology