FDA applicant

Physical Health Devices, Inc.

Miami, FL2 decisions1987–19900 recalls

FDA records 2 decisions for Physical Health Devices, Inc. (Miami, FL) from 1987 to 1990: 2 510(k) clearances. All are in product code HCC (Device, Biofeedback). 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, neurology panel, where it files most

How often FDA has decided Physical Health Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Physical Health Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Physical Health Devices, 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 “Physical”

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

Physical Diagnostics, Inc. 1

Physical Health Devices, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Physical”