# K222127: Soft Palate Elevator

- Pathway: 510(k) (Abbreviated)
- Applicant: The Tmj Clinic PC
- Decided: Oct 24, 2022 after 98 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 K895189 (1990). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K895189: Adjustable Soft Palate Lifter, Ortho Publications, Inc. (1990) Summary page 5.

## Indications for use
TREATMENT OF SNORING

Source page: https://510kreport.com/device/K222127
Methodology: https://510kreport.com/methodology