510(k) Report

FDA applicant

Davis Assoc.

Bridgeport, CT1 decision1988–19880 recalls

FDA records 1 decision for Davis Assoc. (Bridgeport, CT) in 1988: 1 510(k) clearance. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 Davis Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Davis Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Davis Assoc. 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?

  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K880042AcutronDavis Assoc. · 19881cites it

What has FDA decided for it lately?

The one decision as Davis Assoc. →

Other applicant names beginning “Davis”

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

Davis & Geck, Inc. 46Davis Schottlander & Davis, Ltd. 7Davis Lead Aprons, Inc. 3Davis Medical 1Davis-Smith Corp. 1Davis Positioning Systems, Inc. 1