FDA applicant

Larson Medical Products, Inc.

Newark, OH1 decision2011–20110 recalls

FDA records 1 decision for Larson Medical Products, Inc. (Newark, OH) in 2011: 1 510(k) clearance. All are in product code IYE (Accelerator, Linear, Medical). 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, radiology panel, where it files most

How often FDA has decided Larson Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

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

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Other applicant names beginning “Larson”

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

Larson Products, Inc. 1

Larson Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Larson”