510(k) Report

FDA applicant

Human Performance Technologies, Inc.

East Setauket, NY2 decisions1988–19880 recalls

FDA records 2 decisions for Human Performance Technologies, Inc. (East Setauket, NY) in 1988: 2 510(k) clearances. Most are in product codes JFC (System, Pressure Measurement, Intermittent) and LXJ (Interactive Rehabilitation Exercise Devices). 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 Human Performance Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Human Performance Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Human”

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