FDA applicant

Airways Ltd., Inc.

Matawan, NJ2 decisions1997–20040 recalls

FDA records 2 decisions for Airways Ltd., Inc. (Matawan, NJ) from 1997 to 2004: 2 510(k) clearances. Most are in product codes BZD (Ventilator, Non-Continuous (Respirator)) and CBK (Ventilator, Continuous, Facility Use). Its devices cite 6 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, anesthesiology panel, where it files most

How often FDA has decided Airways Ltd., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Airways Ltd., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Airways Ltd., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Airways Ltd., 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 “Airways”

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

Airways Development, LLC 1

Airways Ltd., 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 “Airways”