# K072731: Endsnor

- Pathway: 510(k) (Abbreviated)
- Applicant: Dockstader Orthodontic Lab, Inc.
- Decided: Jun 12, 2008 after 260 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 K955503 (1996). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K955503: Adjustable PM Positioner, Jonathan A. Parker, D.D.S. (1996) Summary page 2.

## Most influential descendants
- K090911: Ist Snoring Appliance (2009), 0 descendants of its own

## Indications for use
The EndSnor TM appliance, a dentist prescribed mandibular repositioning (MRP) device, is worn during sleep and is indicated for persons 18 years or older, who wish to reduce the incidence of snoring and/or mild to moderate obstructive sleep apnea. Before a dentist prescribes an EndSnorT M appliance for treatment, it is recommended that the patient receive a medical examination including a sleep study diagnosis, and a dental examination including cephalometric and tomography analysis to determine the need for an EndSnorTM appliance.

Source page: https://510kreport.com/device/K072731
Methodology: https://510kreport.com/methodology