510(k) Report

FDA applicant

Sense Technology, Inc.

Pittsburgh, PA2 decisions1994–19980 recalls

FDA records 2 decisions for Sense Technology, Inc. (Pittsburgh, PA) from 1994 to 1998: 2 510(k) clearances. All are in product code LXM (Manipulator, Plunger-Like Joint). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sense 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?

  • LXMManipulator, Plunger-Like Joint2decisions

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K973914Sense Technology Inc. Fras, Sense Technology Inc. PulstarSense Technology, Inc. · 19982cite it
  • K940085Force Recording and Analysis System, Model 01Sense Technology, Inc. · 19941cites it

What has FDA decided for it lately?

  • K973914Sense Technology Inc. Fras, Sense Technology Inc. PulstarSense Technology, Inc. · 1998
  • K940085Force Recording and Analysis System, Model 01Sense Technology, Inc. · 1994

All 2 as Sense Technology, Inc. →