FDA applicant

Axon Instruments, Inc.

Foster City, CA3 decisions1997–19990 recalls

FDA records 3 decisions for Axon Instruments, Inc. (Foster City, CA) from 1997 to 1999: 3 510(k) clearances. Most are in product codes GZL (Electrode, Depth) and HAW (Neurological Stereotaxic Instrument). Its devices cite 1 predicate, 0 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, neurology panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Axon 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 “Axon”

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

Axon Systems, Inc. 15 Axon Medical 2 Axon Spine Medical System 1 Axon Medical Technologies Corp. 1

Axon Instruments, 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 “Axon”