510(k) Report

FDA applicant

Preferred Optics, Inc.

Marietta, GA1 decision1994–19940 recalls

FDA records 1 decision for Preferred Optics, Inc. (Marietta, GA) in 1994: 1 510(k) clearance. All are in product code LPL (Lenses, Soft Contact, Daily Wear). 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 Preferred Optics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Preferred Optics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Preferred Optics, 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 “Preferred”

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