510(k) Report

FDA applicant

Lbds Holding Company

Las Vegas, NV1 decision2011–20110 recalls

FDA records 1 decision for Lbds Holding Company (Las Vegas, NV) in 2011: 1 510(k) clearance. All are in product code MOS (Coil, Magnetic Resonance, Specialty). 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 Lbds Holding Company’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011: 1
2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Lbds Holding Company by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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