FDA applicant

Pro-Tec Containers, Inc.

Lake Mary, FL6 decisions1989–19940 recalls

FDA records 6 decisions for Pro-Tec Containers, Inc. (Lake Mary, FL) from 1989 to 1994: 6 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and JKA (Tubes, Vials, Systems, Serum Separators, Blood…). 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 Pro-Tec Containers, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pro-Tec Containers, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Pro-Tec Containers, Inc.

Which product codes does it file in?

What has FDA decided for it lately?