# K093710: The Moses Appliance

- Pathway: 510(k) (Abbreviated)
- Applicant: Allen J. Moses, Dds, Ltd.
- Decided: May 12, 2010 after 161 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K121285: Oravan Osa (2013), 2 descendants of its own
- K152159: Oravan Herbst (2015), 0 descendants of its own
- K130797: Luco Hybrid Osa Appliance (2013), 0 descendants of its own

## Indications for use
The MoseSTm appliance is intended for use on adult patients 18 years of age and older as an aid for the reduction and/or alleviation of snoring and mild to moderate obstructive sleep apnea.

Source page: https://510kreport.com/device/K093710
Methodology: https://510kreport.com/methodology