510(k) Report

FDA applicant

Metrosoft, Inc.

Rosewell, GA2 decisions1995–19980 recalls

FDA records 2 decisions for Metrosoft, Inc. (Rosewell, GA) from 1995 to 1998: 2 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). 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, ophthalmic panel, where it files most

How often FDA has decided Metrosoft, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Metrosoft, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Metrosoft, 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?

  • LPLLenses, Soft Contact, Daily Wear2decisions

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.

  • K953199Metro 55G Toric & SphericalMetrosoft, Inc. · 19952cite it

What has FDA decided for it lately?

  • K983021Metrosoft II, Metrosoft Toric, Metrolite, Metrotint, Satureyes, Satureyes Toric, Satureyes Lite, Satureyes…Metrosoft, Inc. · 1998
  • K953199Metro 55G Toric & SphericalMetrosoft, Inc. · 1995

All 2 as Metrosoft, Inc. →