510(k) Report

FDA applicant

Xylog Corp.

Hackensack, NJ4 decisions1988–19940 recalls

FDA records 4 decisions for Xylog Corp. (Hackensack, NJ) from 1988 to 1994: 4 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and KNS (Unit, Electrosurgical, Endoscopic (With Or…). 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 Xylog Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Xylog Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Xylog 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?

  • GEIElectrosurgical, Cutting & Coagulation & Accessories2decisions
  • KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)1decision
  • FCXInsufflator, Automatic Carbon-Dioxide For Endoscope1decision

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.

  • K882048Meditron Endolav Model EL-100Xylog Corp. · 19881cites it

What has FDA decided for it lately?

  • K945970Insufflator Filter Tubing SetXylog Corp. · 1994
  • K882048Meditron Endolav Model EL-100Xylog Corp. · 1988
  • K882049Meditron MG-1000 Monopolar GeneratorXylog Corp. · 1988
  • K874798Meditron BI-2000 Bipolar Generator W/IrrigationXylog Corp. · 1988

All 4 as Xylog Corp. →