FDA applicant

Cutler & Gross Sloan Optical, Ltd.

England, GB1 decision1991–19910 recalls

FDA records 1 decision for Cutler & Gross Sloan Optical, Ltd. (England, GB) in 1991: 1 510(k) clearance. All are in product code HOI (Spectacle, Magnifying). 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 & Gross Sloan Optical, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cutler & Gross Sloan Optical, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cutler & Gross Sloan Optical, Ltd. 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 Medical Instruments 2 Cutler Biomedical 1

Cutler & Gross Sloan Optical, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cutler”