510(k) Report

FDA applicant

The Lebanon Corp.

Mchenry, IL3 decisions1982–19840 recalls

FDA records 3 decisions for The Lebanon Corp. (Mchenry, IL) from 1982 to 1984: 3 510(k) clearances. Most are in product codes EPT (Microscope, Surgical) and LCC (Applicator, Ocular Pressure). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for The Lebanon Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Lebanon 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?

  • EPTMicroscope, Surgical1decision
  • LCCApplicator, Ocular Pressure1decision

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.

  • K820526Relief Valve-Honan Intraoc. PressureThe Lebanon Corp. · 19821cites it

What has FDA decided for it lately?

  • K841652Ocular Pressure ApplicatorThe Lebanon Corp. · 1984
  • K821689Lebanon MicroscopeThe Lebanon Corp. · 1982
  • K820526Relief Valve-Honan Intraoc. PressureThe Lebanon Corp. · 1982

All 3 as The Lebanon Corp. →

Other applicant names beginning “The”

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

The Lebanon Vac-Tray Corp. 1