510(k) Report

FDA applicant

Rehab Technology, Inc.

Aviston, IL4 decisions1984–19920 recalls

FDA records 4 decisions for Rehab Technology, Inc. (Aviston, IL) from 1984 to 1992: 4 510(k) clearances. Most are in product codes IQA (System, Environmental Control, Powered) and IPL (Wheelchair, Standup). 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 Rehab Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rehab Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rehab Technology, 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?

  • IQASystem, Environmental Control, Powered3decisions
  • IPLWheelchair, Standup1decision

What has FDA decided for it lately?

  • K921084The ExcelsiorRehab Technology, Inc. · 1992
  • K850313Television Control Option 1219Rehab Technology, Inc. · 1985
  • K850314Television Control Option 1220Rehab Technology, Inc. · 1985
  • K840808ECU 1218Rehab Technology, Inc. · 1984

All 4 as Rehab Technology, Inc. →

Other applicant names beginning “Rehab”

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

Rehab Medical Specialties, Inc. 3Rehab 'N Motion Technologies 1Rehab, Inc. 1