# K262104: Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)

- Pathway: 510(k) (Special)
- Applicant: Ram.Shaw Pte., Ltd.
- Decided: Aug 27, 2026 after 65 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: 7 generations back to K071404 (2007). 12 ancestors in all.
No later device cites it as a predicate yet.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K253845: Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB), Ram.Shaw Pte., Ltd. (2026) Summary page 5.

## Indications for use
The anti-snoring mouthpiece is intended to reposition the lower jaw during sleep to help maintain an open airway and reduce snoring in adults aged 18 years or older. The device is intended for over-the-counter home use.

Source page: https://510kreport.com/device/K262104
Methodology: https://510kreport.com/methodology