510(k) Report

FDA applicant

Eye Garter Company, Inc.

Houston, TX6 decisions1988–19900 recalls

FDA records 6 decisions for Eye Garter Company, Inc. (Houston, TX) from 1988 to 1990: 6 510(k) clearances. All are in product code HOY (Shield, Eye, Ophthalmic (Including Sunlamp…). 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 Eye Garter Company, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eye Garter Company, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Eye Garter Company, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Eye Garter Company, Inc.’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?

  • HOYShield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)6decisions

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.

  • K896171Eye PatchEye Garter Company, Inc. · 19891cites it

What has FDA decided for it lately?

  • K900941OmnipatchEye Garter Company, Inc. · 1990
  • K896171Eye PatchEye Garter Company, Inc. · 1989
  • K896172Strapped Eye ShieldEye Garter Company, Inc. · 1989
  • K880489Clear Eye Garter ShieldEye Garter Company, Inc. · 1988
  • K880490Blue Plastic Eye ShieldEye Garter Company, Inc. · 1988
  • K880675Easy Shield Adhesive BandageEye Garter Company, Inc. · 1988

All 6 as Eye Garter Company, Inc. →