FDA applicant

Chiron Intraoptics

Irvine, CA4 decisions1992–19930 recalls

FDA records 4 decisions for Chiron Intraoptics (Irvine, CA) from 1992 to 1993: 4 510(k) clearances. Most are in product codes LYX (Media, Corneal Storage) and HQC (Unit, Phacofragmentation). 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 Intraoptics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Chiron Intraoptics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Chiron Intraoptics’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 Ophthalmics 11 Chiron Corp. 2

Chiron Intraoptics

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”