# K152159: Oravan Herbst

- Pathway: 510(k) (Traditional)
- Applicant: Oravanosa, LLC
- Decided: Oct 29, 2015 after 87 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). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130558: Somnodent Herbst; Classic, Flex, Somnomed, Inc. (2013) Summary page 5.
- K121285: Oravan Osa, New Jersey Snoring Solutions (2013) Summary page 5.

## Indications for use
Oravan Herbst is intended to reduce snoring and mild to moderate sleep apnea in adults.

Source page: https://510kreport.com/device/K152159
Methodology: https://510kreport.com/methodology