510(k) Report

FDA applicant

Surgilight, Inc.

Orlando, FL2 decisions2000–20020 recalls

FDA records 2 decisions for Surgilight, Inc. (Orlando, FL) from 2000 to 2002: 2 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Surgilight, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Surgilight, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Surgilight, Inc. 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 Instrument2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K020973EX-308 Excimer Laser for Phototherapy Treatment of VitiligoSurgilight, Inc. · 20021cites it
  • K993328Surgilight, Inc Excimer LaserSurgilight, Inc. · 20001cites it

What has FDA decided for it lately?

  • K020973EX-308 Excimer Laser for Phototherapy Treatment of VitiligoSurgilight, Inc. · 2002
  • K993328Surgilight, Inc Excimer LaserSurgilight, Inc. · 2000

All 2 as Surgilight, Inc. →