510(k) Report

FDA applicant

Super Optical, Inc.

Hialeah, FL1 decision1994–19940 recalls

FDA records 1 decision for Super Optical, Inc. (Hialeah, FL) in 1994: 1 510(k) clearance. All are in product code HQZ (Frame, Spectacle). 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 Super Optical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Super Optical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Super Optical, 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?

  • HQZFrame, Spectacle1decision

What has FDA decided for it lately?

  • K940977Spectacle FramesSuper Optical, Inc. · 1994

The one decision as Super Optical, Inc. →

Other applicant names beginning “Super”

FDA records each applicant name separately; these may or may not be the same firm.

Super Safe Plastic Products Co., Ltd. 6Super Grow Lasers 2Super Sagless Corp. 2Super Glide, Inc. 2