FDA applicant

Laerdal California, Inc.

Long Beach, CA5 decisions1983–19940 recalls

FDA records 5 decisions for Laerdal California, Inc. (Long Beach, CA) from 1983 to 1994: 5 510(k) clearances. Most are in product codes BTA (Pump, Portable, Aspiration (Manual Or Powered)) and IQK (Orthosis, Cervical). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Laerdal California, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Laerdal California, Inc. 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 Mfg. Corp. 5 Laerdal Medical A/S 4

Laerdal California, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Laerdal”