FDA applicant

Medical Products, Inc.

Chantilly, VA2 decisions1998–20130 recalls

FDA records 2 decisions for Medical Products, Inc. (Chantilly, VA) from 1998 to 2013: 2 510(k) clearances. Most are in product codes LGZ (Warmer, Thermal, Infusion Fluid) and NFB (Conserver, Oxygen). No recall is linked to its devices.

FDA’s records also spell it “Medical Products, LLC”.

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

FDA decisions per year

1in 2013

2007high 1 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?