# K252374: Nylon flexTAP (R)

- Pathway: 510(k) (Special)
- Applicant: Airway Technologies D/B/A Airway Management
- Decided: Sep 11, 2025 after 43 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). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061732: TAP-T, Airway Management, Inc. (2006) Summary page 5.

## Indications for use
The Nylon flexTAP is intended to reduce or alleviate nighttime snoring and mild to moderate obstructive sleep apnea, OSA for adults, 18 years of age and older.

Source page: https://510kreport.com/device/K252374
Methodology: https://510kreport.com/methodology