510(k) Report

FDA applicant

Esp Plastics, Inc.

Mchenry, IL4 decisions1982–19820 recalls

FDA records 4 decisions for Esp Plastics, Inc. (Mchenry, IL) in 1982: 4 510(k) clearances. Most are in product codes BTC (Bag, Reservoir) and CAE (Airway, Oropharyngeal, Anesthesiology). 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, anesthesiology panel, where it files most

How often FDA has decided Esp Plastics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Esp Plastics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Esp Plastics, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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