# K090436: Airwayease Mas

- Pathway: 510(k) (Traditional)
- Applicant: Orthoplant Dental Lab
- Decided: Apr 16, 2010 after 421 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: 5 generations back to K882303 (1989). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073004: Somnomed  Bflex, Somnomed, Inc. (2008) Summary page 1.

## Indications for use
The Airwayease MIAS is intended to reduce or alleviate night time snoring and mild to moderate obstructive sleep apnea (OSA).

Source page: https://510kreport.com/device/K090436
Methodology: https://510kreport.com/methodology