FDA applicant

Medical Positioning, Inc.

Lake Forest, CA3 decisions2001–20090 recalls

FDA records 3 decisions for Medical Positioning, Inc. (Lake Forest, CA) from 2001 to 2009: 3 510(k) clearances. All are in product code DPS (Electrocardiograph). Its devices cite 2 predicates, 2 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, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2009

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Positioning, Inc.

Which product codes does it file in?

Which of its devices are cited most?

What has FDA decided for it lately?