FDA applicant

Lucas Sensing Systems, Inc.

Phoenix, AZ1 decision1991–19910 recalls

FDA records 1 decision for Lucas Sensing Systems, Inc. (Phoenix, AZ) in 1991: 1 510(k) clearance. All are in product code KQX (Goniometer, Ac-Powered). 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, orthopedic panel, where it files most

How often FDA has decided Lucas Sensing Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lucas Sensing Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lucas Sensing Systems, 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 “Lucas”

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

Lucas Medical, Inc. 7 Lucas Grason-Stadler, Inc. 3 Lucas Lifecare 2 Lucas & Rhea Mfg. 1

Lucas Sensing Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lucas”