# K022284: Snore-Aid Max

- Pathway: 510(k) (Traditional)
- Applicant: Dental Imagineers, LLC
- Decided: Dec 10, 2002 after 148 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: 2 generations back to K882303 (1989). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K991449: Snore-Aid Plus, Dental Imagineers, LLC (1999) Summary page 1.
- K962516: Tap Anti-Snoring Device, Nellcor Puritan Bennett, Inc. (1996) Summary page 1.
- K882303: H&M Anti-Snoring Device, Hays & Meade, Inc. (1989)

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

Source page: https://510kreport.com/device/K022284
Methodology: https://510kreport.com/methodology