FDA applicant

Pulse Medical Instruments

Costa Mesa, CA1 decision1989–19890 recalls

FDA records 1 decision for Pulse Medical Instruments (Costa Mesa, CA) in 1989: 1 510(k) clearance. All are in product code HLG (Pupillometer, Ac-Powered). 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 Pulse Medical Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pulse Medical Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Pulse”

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

Pulse Biosciences, Inc. 7 Pulse Time Products, Ltd. 6 Pulse Metric, Inc. 5 Pulse Biomedical, Inc. 3 Pulse Scientific, Inc. 3 Pulse Life, Inc. 1 Pulse Med, Inc. 1

Pulse Medical Instruments

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pulse”