FDA applicant

Varian, Inc.

Lake Forest, CA5 decisions2004–20060 recalls

FDA records 5 decisions for Varian, Inc. (Lake Forest, CA) from 2004 to 2006: 5 510(k) clearances. Most are in product codes DKZ (Enzyme Immunoassay, Amphetamine) and DJC (Thin Layer Chromatography, Methamphetamine). Its devices cite 7 predicates, 2 of them its own earlier devices. 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, clinical toxicology panel, where it files most

How often FDA has decided Varian, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Varian, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Varian, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Varian”

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

Varian Medical Systems, Inc. 206 Varian Assoc., Inc. 86 Varian Canada, Inc. 7 Varian Medical Systems, Oncology Systems 4 Varian Medical Systems, X-Ray Products-Infimed 2

Varian, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Varian”