# K880956: Snoar (TM) Open Airway Appliance

- Pathway: 510(k) (Traditional)
- Applicant: Kent J. Toone, D.D.S.
- Decided: May 11, 1988 after 65 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.
36 later devices descend from it; 1 cites it directly.
0 of 37 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K971794: Elastic Mandibular Advancement (Ema) Appliance (1997), 35 descendants of its own
- K113201: Narval CC (2011), 15 descendants of its own
- K013808: Sleepbite (2002), 11 descendants of its own
- K143244: The Panthera Anti-Snoring Device (2014), 9 descendants of its own
- K052862: Full Breath Sleep Appliance - AB (Anterior Bite) (2005), 9 descendants of its own

Source page: https://510kreport.com/device/K880956
Methodology: https://510kreport.com/methodology