510(k) Report

FDA applicant

Advanced Rehabilitative Technology, Inc.

San Antonio, TX3 decisions1991–19930 recalls

FDA records 3 decisions for Advanced Rehabilitative Technology, Inc. (San Antonio, TX) from 1991 to 1993: 3 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and IKE (Transducer, Miniature Pressure). 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 Advanced Rehabilitative Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Rehabilitative Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Advanced Rehabilitative 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?

  • IPFStimulator, Muscle, Powered2decisions
  • IKETransducer, Miniature Pressure1decision

What has FDA decided for it lately?

  • K915369The EqualizerAdvanced Rehabilitative Technology, Inc. · 1993
  • K912328Electronic Muscle Stimulators, Excel II, ModifiedAdvanced Rehabilitative Technology, Inc. · 1992
  • K903711Rheologic IAdvanced Rehabilitative Technology, Inc. · 1991

All 3 as Advanced Rehabilitative Technology, Inc. →