510(k) Report

FDA applicant

Cardon Rehabilitation Products, Inc.

Niagara Falls, NY16 decisions1995–19960 recalls

FDA records 16 decisions for Cardon Rehabilitation Products, Inc. (Niagara Falls, NY) from 1995 to 1996: 16 510(k) clearances. All are in product code INQ (Table, Powered). 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 Cardon Rehabilitation Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cardon Rehabilitation Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cardon Rehabilitation 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?

  • INQTable, Powered16decisions

What has FDA decided for it lately?

  • K960336Cardon Physical Therapy Table Model R27645Cardon Rehabilitation Products, Inc. · 1996
  • K960332Cardon Physical Therapy Table Model R28598Cardon Rehabilitation Products, Inc. · 1996
  • K960334Cardon Physical Therapy Table Model R27116Cardon Rehabilitation Products, Inc. · 1996
  • K951955Cardon Physical Therapy Table Model:R40194Cardon Rehabilitation Products, Inc. · 1995
  • K951906Cardon Physical Therapy Tables Models R28591 & R28592Cardon Rehabilitation Products, Inc. · 1995
  • K951952Cardon Physical Therapy Table Model R27112Cardon Rehabilitation Products, Inc. · 1995
  • K951953Cardon Phsical Therapy Table Model R27630Cardon Rehabilitation Products, Inc. · 1995
  • K951954Cardon Physical Therapy Table Model R27108Cardon Rehabilitation Products, Inc. · 1995

All 16 as Cardon Rehabilitation Products, Inc. →