# K053065: Full Breath Sleep Appliance - PB (Posterior Bite and PBB (Posterior Bite with Bumps)

- Pathway: 510(k) (Traditional)
- Applicant: Bryan Keropian Dds
- Decided: Jan 3, 2006 after 63 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
Longest line of descent: 1 generation back to K032410 (2005). 1 ancestor in all.
9 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032410: Snorenti, James P Boyd (2005) Summary page 2.

## Most influential descendants
- 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
- K182312: Zyppah Anti-Snoring Device (2019), 3 descendants of its own
- K252531: Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2) (2026), 1 descendant of its own

## Indications for use
An oral appliance to be used for the treatment of mild and moderate Obstructive Sleep Apnea. For the treatment of snoring. For the prevention of bruxism.

Source page: https://510kreport.com/device/K053065
Methodology: https://510kreport.com/methodology