510(k) Report

FDA applicant

Golden Vision, Inc.

Miami, FL1 decision1999–19990 recalls

FDA records 1 decision for Golden Vision, Inc. (Miami, FL) in 1999: 1 510(k) clearance. All are in product code HKY (Tonometer, Manual). 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 Golden Vision, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Golden Vision, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Golden Vision, 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?

  • HKYTonometer, Manual1decision

Who builds on its devices?

Later devices cite its devices 10 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.

  • K981432Goldman Manual TonometerGolden Vision, Inc. · 199910cite it

What has FDA decided for it lately?

  • K981432Goldman Manual TonometerGolden Vision, Inc. · 1999

The one decision as Golden Vision, Inc. →

Other applicant names beginning “Golden”

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

Golden Technologies, Inc. 8Golden Horse Medical Equipment (Wuxi) Co., Ltd. 2Golden Year Supply Co. 2Golden Bonanza Industrial Corp. 1Golden Dental Products, Inc. 1Golden Bridge International, Inc. 1Golden Motor Technology Co., Ltd. 1Golden Charter, Ltd. 1Golden Gloves Intl. 1Golden Earth Corp. 1Golden State Audiology Assoc. 1Golden Hit, Ltd. 1