# K102521: Pantino Pro Positiner

- Pathway: 510(k) (Traditional)
- Applicant: Somnomed, Inc.
- Decided: Mar 28, 2011 after 207 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: 7 generations back to K882303 (1989). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050592: Somnomed Mas Rxa, Somnomed, Ltd. (2005) Summary page 1.
- K061732: TAP-T, Airway Management, Inc. (2006) Summary page 1.
- K062951: Tap Iii Anti-Snoring Device, Airway Management, Inc. (2006) Summary page 1.

## Indications for use
The Pantino Pro Positioner is intended for the treatment of nighttime snoring and mild to moderate obstructive sleep apnea in patients 18 years of age or older.

Source page: https://510kreport.com/device/K102521
Methodology: https://510kreport.com/methodology