FDA applicant

Molloy Corp.

Lebanon, PA1 decision1996–19960 recalls

FDA records 1 decision for Molloy Corp. (Lebanon, PA) in 1996: 1 510(k) clearance. All are in product code BSR (Stylet, Tracheal Tube). 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 Molloy Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Molloy Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Molloy Corp.

Which product codes does it file in?

What has FDA decided for it lately?