510(k) Report

FDA applicant

Lc Ent.

Cincinnati, OH1 decision1993–19930 recalls

FDA records 1 decision for Lc Ent. (Cincinnati, OH) in 1993: 1 510(k) clearance. All are in product code GEX (Powered Laser Surgical Instrument). 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 Lc Ent.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lc Ent. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lc Ent. 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?

  • GEXPowered Laser Surgical Instrument1decision

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.

  • K932272Closed End/Electrocautery Fiberopt Laser Deliv SysLc Ent. · 19931cites it

What has FDA decided for it lately?

  • K932272Closed End/Electrocautery Fiberopt Laser Deliv SysLc Ent. · 1993

The one decision as Lc Ent. →