510(k) Report

FDA applicant

Polymer Technologies

Whitwater, WI1 decision1986–19860 recalls

FDA records 1 decision for Polymer Technologies (Whitwater, WI) in 1986: 1 510(k) clearance. All are in product code KNT (Tubes, Gastrointestinal (And Accessories)). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Polymer Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Polymer Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • KNTTubes, Gastrointestinal (And Accessories)1decision

What has FDA decided for it lately?

  • K861494Empty Solution Transfer Container 1,500 MLPolymer Technologies · 1986

The one decision as Polymer Technologies →

Other applicant names beginning “Polymer”

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

Polymer Technology Corp. 28Polymer Technology Systems, Inc. 27Polymer Technology Intl. 6Polymer Technology Systems, Inc. D/B/A Pts Diagnostics 3Polymer Technology Div. Wilmington Partners, L.P. 3