# K210910: Snore Bandit

- Pathway: 510(k) (Traditional)
- Applicant: Snorebandit, LLC
- Decided: Jul 1, 2021 after 94 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: 8 generations back to K882303 (1989). 25 ancestors in all.
No later device cites it as a predicate yet.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K191618: SleepTight Mouthpiece STZ, Michael D Williams Dds PA (2019) Summary page 4.
- K190058: PureSleep (OTC use), Sleep Science Partners, Inc. (2019) Summary page 4.
- K180124: ZQuiet, Sleeping Well, LLC (2018) Summary page 4.

## Indications for use
Snore Bandit is intended for use by adult patients (18 years or older) as an aid to reduce snoring.

Source page: https://510kreport.com/device/K210910
Methodology: https://510kreport.com/methodology