FDA applicant

Chiron Ophthalmics

Irvine, CA11 decisions1988–19920 recalls

FDA records 11 decisions for Chiron Ophthalmics (Irvine, CA) from 1988 to 1992: 10 510(k) clearances and 1 original PMA approval. Most are in product codes MOE (Collagen Corneal Shield) and HQL (Intraocular 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 Chiron Ophthalmics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Chiron Ophthalmics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Chiron 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 “Chiron”

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

Chiron Vision Corp. 34 Chiron Diagnostics Corp. 20 Chiron Intraoptics 4 Chiron Corp. 2

Chiron Ophthalmics

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Chiron”