510(k) Report

FDA applicant

Buckman Consultants

Mchenry, IL3 decisions1982–19830 recalls

FDA records 3 decisions for Buckman Consultants (Mchenry, IL) from 1982 to 1983: 3 510(k) clearances. Most are in product codes KNX (Collector, Urine, (And Accessories) For…) and IPY (Orthosis, Lumbo-Sacral). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Buckman Consultants since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Buckman Consultants 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?

  • KNXCollector, Urine, (And Accessories) For Indwelling Catheter1decision
  • IPYOrthosis, Lumbo-Sacral1decision
  • BXBExerciser, Powered1decision

What has FDA decided for it lately?

  • K830316UniflexBuckman Consultants · 1983
  • K823882M-BraceBuckman Consultants · 1983
  • K821829UrogardBuckman Consultants · 1982

All 3 as Buckman Consultants →

Other applicant names beginning “Buckman”

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

Buckman Co., Inc. 111