FDA applicant

Sleep Science Partners, Inc.

Larkspur, CA2 decisions2012–20190 recalls

FDA records 2 decisions for Sleep Science Partners, Inc. (Larkspur, CA) from 2012 to 2019: 2 510(k) clearances. All are in product code LRK (Device, Anti-Snoring). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Science Partners, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Sleep Science Partners, Inc. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sleep Science Partners, 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 Solutions, Inc. 2 Sleep Specialists, LLC 1 Sleep Medicine Network, Inc. 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 Science Partners, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Sleep”