FDA applicant

Medical Safety Products, Inc.

Denver, CO6 decisions1988–19940 recalls

FDA records 6 decisions for Medical Safety Products, Inc. (Denver, CO) from 1988 to 1994: 6 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and FOZ (Catheter, Intravascular, Therapeutic…). 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 Medical Safety Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Safety Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Safety Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?