FDA applicant

Physio Technology, Inc.

Topeka, KS10 decisions1984–19880 recalls

FDA records 10 decisions for Physio Technology, Inc. (Topeka, KS) from 1984 to 1988: 10 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and IMG (Stimulator, Ultrasound And Muscle, For Use In…). 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 Physio Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Physio Technology, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Physio”

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

Physio-Control Corp. 97 Physio Systems, Inc. 3 Physio Tronics Corp. 1 Physio Designs, Inc. 1 Physio-Dyne Industrument Corp. 1 Physio-Dyne 1 Physio-Dyne Instrument Corp. 1 Physio, Inc. 1 Physio Ventures, Inc. 1

Physio Technology, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Physio”