FDA applicant

Cutler Medical Instruments

Santa Monica, CA2 decisions1985–19860 recalls

FDA records 2 decisions for Cutler Medical Instruments (Santa Monica, CA) from 1985 to 1986: 2 510(k) clearances. Most are in product codes HLR (Keratoscope, Battery-Powered) and HQE (Instrument, Vitreous Aspiration And Cutting…). 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 Cutler Medical Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cutler Medical Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cutler 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 “Cutler”

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

Cutler Laboratories, Inc. 2 Cutler & Gross Sloan Optical, Ltd. 1 Cutler Biomedical 1

Cutler Medical Instruments

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cutler”