# K143244: The Panthera Anti-Snoring Device

- Pathway: 510(k) (Traditional)
- Applicant: Panthera Dental, Inc.
- Decided: Dec 15, 2014 after 33 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: 5 generations back to K882303 (1989). 9 ancestors in all.
9 later devices descend from it; 5 cite it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113201: Narval CC, Resmed Sas (2011) Summary page 5.

## Most influential descendants
- K203596: Panthera Occlusal Appliance (2021), 2 descendants of its own
- K232025: Hushd Pro Avera (2024), 1 descendant of its own
- K230495: Serena Sleep Night Guard (2023), 1 descendant of its own
- K171576: The Panthera Anti-Snoring X3 Device (2018), 1 descendant of its own
- K252976: Park Dental Nylon MAD (2025), 0 descendants of its own

## Indications for use
The Panthera Anti-Snoring Device is intended to reduce or alleviate snoring and mild to moderate obstructive sleep apnea (OSA) in adults.

Source page: https://510kreport.com/device/K143244
Methodology: https://510kreport.com/methodology