# K231663: The AVEOtsd (Tongue Stabilizing Device) Mouthpiece

- Pathway: 510(k) (Traditional)
- Applicant: Innovative Health Technologies (Nz), Ltd.
- Decided: Sep 18, 2023 after 103 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K252531: Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2) (2026), 1 descendant of its own
- K261912: SnØreNegatØr (2026), 0 descendants of its own

## Indications for use
The AVEOtsd (Tongue Stabilizing Device) Mouthpiece is intended as an aid in the reduction of snoring for adults at least 18 years old.

Source page: https://510kreport.com/device/K231663
Methodology: https://510kreport.com/methodology