FDA applicant

Norton Performance Plastics Corp.

Mchenry, IL39 decisions1977–19850 recalls

FDA records 39 decisions for Norton Performance Plastics Corp. (Mchenry, IL) from 1977 to 1985: 39 510(k) clearances. Most are in product codes DYB (Introducer, Catheter) and DQO (Catheter, Intravascular, Diagnostic). 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, cardiovascular panel, where it files most

How often FDA has decided Norton Performance Plastics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Norton Performance Plastics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Norton”

FDA records each applicant name separately; these may or may not be the same firm.

Norton Texas Medical Products 4

Norton Performance Plastics Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Norton”