# K081965: Mpowrx Snoring Solution

- Pathway: 510(k) (Traditional)
- Applicant: Mpowrx Health and Wellness Products, Inc.
- Decided: Oct 27, 2008 after 109 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 K954324 (1995). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954324: Snor-X Mouth Guard, Snorex, Inc. (1995) Summary page 1.
- K993381: Tongue Stabilizer Device, University of Otago (1999) Summary page 1.
- K013687: Nose Breathe Mouthpiece for Heavy Snorer, Steven K. Sue (2002) Summary page 1.

## Most influential descendants
- K172991: Advanced Dental Applicance (2018), 1 descendant of its own
- K203462: Advanced Dental Appliance (2021), 0 descendants of its own

## Indications for use
The MPowRxTM Snoring Solution is intended for the treatment of mild to moderate snoring.

Source page: https://510kreport.com/device/K081965
Methodology: https://510kreport.com/methodology