FDA applicant

Sola Ophthalmics

Phoenix, AZ1 decision1987–19870 recalls

FDA records 1 decision for Sola Ophthalmics (Phoenix, AZ) in 1987: 1 510(k) clearance. All are in product code LRX (Case, Contact Lens). 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 Sola Ophthalmics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sola Ophthalmics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sola Ophthalmics’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 “Sola”

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

Sola-Tan Intl. 3 Sola Medical Devices, LLC 1 Sola-Syntex Ophthalmics 1

Sola Ophthalmics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sola”