FDA applicant

Sleep Medicine Network, Inc.

Portland, OR1 decision2010–20100 recalls

FDA records 1 decision for Sleep Medicine Network, Inc. (Portland, OR) in 2010: 1 510(k) clearance. All are in product code LRK (Device, Anti-Snoring). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Sleep Medicine Network, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Sleep Medicine Network, Inc. by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sleep Medicine Network, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Sleep”

FDA records each applicant name separately; these may or may not be the same firm.

Sleep Science Partners, Inc. 2 Sleep Solutions, Inc. 2 Sleep Specialists, LLC 1 Sleep Specialties, LLC 1 Sleep Group Solutions 1 Sleep Renewal, Inc. 1 Sleep Modus, Inc. 1 Sleep Devices, Inc. 1 Sleep Performance D.B.A. Fatigue Science 1

Sleep Medicine Network, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sleep”