510(k) Report

FDA applicant

Cosmos Medical Technology

Temecula, CA3 decisions1998–20000 recalls

FDA records 3 decisions for Cosmos Medical Technology (Temecula, CA) from 1998 to 2000: 3 510(k) clearances. 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 Cosmos Medical Technology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cosmos Medical Technology since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cosmos Medical Technology by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cosmos Medical Technology’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • GEXPowered Laser Surgical Instrument3decisions

Who builds on its devices?

Later devices cite its devices 6 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.

  • K001784Viridis LaserCosmos Medical Technology · 20002cite it
  • K001704ATHOSCosmos Medical Technology · 20002cite it
  • K983020Compact KTP LaserCosmos Medical Technology · 19982cite it

What has FDA decided for it lately?

  • K001784Viridis LaserCosmos Medical Technology · 2000
  • K001704ATHOSCosmos Medical Technology · 2000
  • K983020Compact KTP LaserCosmos Medical Technology · 1998

All 3 as Cosmos Medical Technology →