FDA applicant

Marine Polymer Technologies, Inc.

Danvers, MA10 decisions1997–20160 recalls

FDA records 10 decisions for Marine Polymer Technologies, Inc. (Danvers, MA) from 1997 to 2016: 10 510(k) clearances. Most are in product codes FRO (Dressing, Wound, Drug) and KMF (Bandage, Liquid). Its devices cite 23 predicates, 6 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Marine Polymer Technologies”.

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 Marine Polymer Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2007high 1 (2007) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Marine Polymer Technologies, 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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Marine Polymer Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?