FDA applicant

Medspring Group, Incorporated

Bountiful, UT1 decision2004–20040 recalls

FDA records 1 decision for Medspring Group, Incorporated (Bountiful, UT) in 2004: 1 510(k) clearance. All are in product code FXX (Mask, Surgical). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Medspring Group, Incorporated since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medspring Group, Incorporated

Which product codes does it file in?

What has FDA decided for it lately?