FDA applicant

Respire Medical

Woodland Hills, CA3 decisions2011–20220 recalls

FDA records 3 decisions for Respire Medical (Woodland Hills, CA) from 2011 to 2022: 3 510(k) clearances. All are in product code LRK (Device, Anti-Snoring). Its devices cite 7 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Respire Medical, LLC”.

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 Respire Medical’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Respire Medical by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Respire Medical’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 “Respire”

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

Respire Medical Holding 3 Respire Medical Holdings 1

Respire Medical

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 “Respire”