510(k) Report

FDA applicant

Young and Moore Enterprises, Inc.

Phoenix, AZ1 decision1987–19870 recalls

FDA records 1 decision for Young and Moore Enterprises, Inc. (Phoenix, AZ) in 1987: 1 510(k) clearance. All are in product code LPN (Accessories, Soft Lens Products). 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 Young and Moore Enterprises, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Young and Moore Enterprises, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Young”

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