FDA applicant

Laerdal Mfg. Corp.

Portland, OR5 decisions1988–19900 recalls

FDA records 5 decisions for Laerdal Mfg. Corp. (Portland, OR) from 1988 to 1990: 5 510(k) clearances. Most are in product codes LDD (Dc-Defibrillator, Low-Energy, (Including…) and MKJ (Automated External Defibrillators (Non-Wearable)). 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, cardiovascular panel, where it files most

How often FDA has decided Laerdal Mfg. Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laerdal Mfg. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Laerdal”

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

Laerdal Medical Corp. 16 Laerdal California, Inc. 5 Laerdal Medical A/S 4

Laerdal Mfg. Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Laerdal”