510(k) Report

FDA applicant

Florida Probe Corp.

Gainesville, FL2 decisions1988–19890 recalls

FDA records 2 decisions for Florida Probe Corp. (Gainesville, FL) from 1988 to 1989: 2 510(k) clearances. Most are in product codes EIL (Gauge, Depth, Instrument, Dental) and EIX (Probe, Periodontic). 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, dental panel, where it files most

How often FDA has decided Florida Probe Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Florida Probe Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Florida Probe Corp. 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?

  • EILGauge, Depth, Instrument, Dental1decision
  • EIXProbe, Periodontic1decision

Who builds on its devices?

Later devices cite its devices 2 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.

  • K875076Florida ProbeFlorida Probe Corp. · 19882cite it

What has FDA decided for it lately?

  • K890493Florida Probe Periodontal ProbeFlorida Probe Corp. · 1989
  • K875076Florida ProbeFlorida Probe Corp. · 1988

All 2 as Florida Probe Corp. →