510(k) Report

FDA applicant

Brady Medical Products Co.

Milwaukee, WI5 decisions1992–19950 recalls

FDA records 5 decisions for Brady Medical Products Co. (Milwaukee, WI) from 1992 to 1995: 5 510(k) clearances. Most are in product codes NAE (Dressing, Wound, Hydrogel Without Drug And/Or…) and KMF (Bandage, Liquid). 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 and plastic surgery panel, where it files most

How often FDA has decided Brady Medical Products Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Brady Medical Products Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Brady Medical Products Co. 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?

  • NAEDressing, Wound, Hydrogel Without Drug And/Or Biologic4decisions
  • KMFBandage, Liquid1decision

What has FDA decided for it lately?

  • K945832Brady Medical Products Transcorbent and Thinsite Topical Border Wound DressingsBrady Medical Products Co. · 1995
  • K941019Brady Medical Products Transorbents Wound DressingBrady Medical Products Co. · 1994
  • K936052Brady Medical Products Hysorb (TM) Wound DressingBrady Medical Products Co. · 1994
  • K935848Brady Medical Products Transorb Wound DressingBrady Medical Products Co. · 1994
  • K922666Transorb (TM) Ulcer & Wound DressingBrady Medical Products Co. · 1992

All 5 as Brady Medical Products Co. →