510(k) Report

FDA applicant

Golden Dental Products, Inc.

Golden, CO1 decision1985–19850 recalls

FDA records 1 decision for Golden Dental Products, Inc. (Golden, CO) in 1985: 1 510(k) clearance. All are in product code NJH (Lens, Spectacle (Prescription), For Reading…). 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 Dental Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Golden Dental Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Golden”

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