FDA applicant

Scieran Technologies, Inc.

Laguna Hills, CA5 decisions1996–19980 recalls

FDA records 5 decisions for Scieran Technologies, Inc. (Laguna Hills, CA) from 1996 to 1998: 5 510(k) clearances. Most are in product codes HQC (Unit, Phacofragmentation) and MRH (Pump, Infusion, 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 Scieran Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Scieran Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Scieran Technologies, Inc.

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?