# K032410: Snorenti

- Pathway: 510(k) (Traditional)
- Applicant: James P Boyd
- Decided: Feb 28, 2005 after 574 days
- Product code: LQZ (Device, Jaw Repositioning)
- 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.
11 later devices descend from it; 4 cite it directly.
0 of 12 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
- K053065: Full Breath Sleep Appliance - PB (Posterior Bite and PBB (Posterior Bite with Bumps) (2006), 9 descendants of its own
- K052862: Full Breath Sleep Appliance - AB (Anterior Bite) (2005), 9 descendants of its own
- K061228: Full Breath Sleep Appliance with Posterior Tongue Depressor (2006), 8 descendants of its own
- K091035: Full Breath Sleep Appliance Lower (FBSL) (2009), 7 descendants of its own
- K111680: DR. Greensburg's Hybrid (2011), 6 descendants of its own

## Indications for use
1. Quiet Night - This appliance is indicated for the treatment of mild to moderate obstructive sleep apnea. 2. Quiet Night MA - This appliance is indicated for the treatment of mild to moderate obstructive sleep apnea. This appliance is intended for use when the Quiet Night is ineffective.

Source page: https://510kreport.com/device/K032410
Methodology: https://510kreport.com/methodology