FDA applicant

Globalmedia Group, LLC

Scottsdale, AZ1 decision2013–20130 recalls

FDA records 1 decision for Globalmedia Group, LLC (Scottsdale, AZ) in 2013: 1 510(k) clearance. All are in product code PEQ (Accessories To Examination Light). 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 hospital panel, where it files most

How often FDA has decided Globalmedia Group, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Globalmedia Group, LLC by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Globalmedia Group, LLC

Which product codes does it file in?

What has FDA decided for it lately?