510(k) Report

FDA applicant

Surgical Products Corp.

Mchenry, IL6 decisions1984–19920 recalls

FDA records 6 decisions for Surgical Products Corp. (Mchenry, IL) from 1984 to 1992: 6 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and 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 Surgical Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Surgical Products Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Surgical Products 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
  • GEXPowered Laser Surgical Instrument1decision
  • FZTCutter, Surgical1decision
  • HRXArthroscope1decision

Who builds on its devices?

Later devices cite its devices 3 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.

  • K921671Surgilase Fiberlase VCO2 Laser WaveguideSurgical Products Corp. · 19923cite it

What has FDA decided for it lately?

  • K921671Surgilase Fiberlase VCO2 Laser WaveguideSurgical Products Corp. · 1992
  • K861614Ghi Wet PencilSurgical Products Corp. · 1986
  • K841241Anterior Cruciate Ligament GrasperSurgical Products Corp. · 1985
  • K841328SPC Arthroscopy TableSurgical Products Corp. · 1984
  • K841247SPC Disposable CutterSurgical Products Corp. · 1984
  • K834434Mach I Electrosurgery Hand ControlSurgical Products Corp. · 1984

All 6 as Surgical Products Corp. →