FDA applicant

Human Technologies, Inc.

St. Petersburg, FL3 decisions1987–19880 recalls

FDA records 3 decisions for Human Technologies, Inc. (St. Petersburg, FL) from 1987 to 1988: 3 510(k) clearances. Most are in product codes KMI (Monitor, Bed Patient) and FLL (Continuous Measurement Thermometer). 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, general hospital panel, where it files most

How often FDA has decided Human Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Human Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Human Technologies, 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 “Human”

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

Human Xtensions, Ltd. 5 Human Performance Technologies, Inc. 2 Human Med AG 2 Human Biosciences, Inc. 2 Human Design Medical, LLC 1 Human Extension, Ltd. 1

Human Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Human”