510(k) Report

FDA applicant

Devon Safety Products, Inc.

Stillwater, MN2 decisions2005–20060 recalls

FDA records 2 decisions for Devon Safety Products, Inc. (Stillwater, MN) from 2005 to 2006: 2 510(k) clearances. Most are in product codes MEG (Syringe, Antistick) and FMF (Syringe, Piston). Its devices cite 4 predicates, 0 of them its own earlier devices. 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, general hospital panel, where it files most

How often FDA has decided Devon Safety Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Devon Safety Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Devon Safety Products, Inc. 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?

  • MEGSyringe, Antistick1decision
  • FMFSyringe, Piston1decision

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K060668Safe Tip SyringeDevon Safety Products, Inc. · 2006
  • K052551Devon Standard Syringe, Hypodermic Needle and Insulin SyringeDevon Safety Products, Inc. · 2005

All 2 as Devon Safety Products, Inc. →

Other applicant names beginning “Devon”

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

Devon Industries, Inc. 47Devon Medical, Inc. 13Devon Medical Products 6Devon Medical Products (Jiangsu), Ltd. 6