FDA applicant

Solos Ophthalmology

Norcross, GA5 decisions1987–19880 recalls

FDA records 5 decisions for Solos Ophthalmology (Norcross, GA) from 1987 to 1988: 5 510(k) clearances. Most are in product codes HQC (Unit, Phacofragmentation) and HMT (Drape, Patient, Ophthalmic). 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 Solos Ophthalmology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Solos Ophthalmology since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Solos Ophthalmology’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 “Solos”

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

Solos Endoscopy, Inc. 21 Solos Mfg. 1

Solos Ophthalmology

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Solos”