FDA applicant

Horiba Instruments, Inc.

Irvine, CA5 decisions1984–19850 recalls

FDA records 5 decisions for Horiba Instruments, Inc. (Irvine, CA) from 1984 to 1985: 5 510(k) clearances. Most are in product codes CEM (Electrode, Ion Specific, Potassium) and JGS (Electrode, Ion Specific, Sodium). 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 chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Horiba Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Horiba”

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

Horiba Abx 37 Horiba, Ltd. 2

Horiba Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Horiba”