510(k) Report

FDA applicant

Superior Plastic Products Corp.

Mchenry, IL15 decisions1976–19852 recalls

FDA records 15 decisions for Superior Plastic Products Corp. (Mchenry, IL) from 1976 to 1985: 15 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and JOL (Catheter And Tip, Suction). 2 recalls are linked to its devices, 1 Class I.

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 Superior Plastic Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Superior Plastic Products Corp. since 2007.

Recalls per year

1in 2023

2013: 12023: 1, 1 Class I
2007high 1 (2013) · low 0 (2007)2026

Class I Class II/III not classified

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

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