FDA applicant

Fine-Cut Diamond Instruments

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Fine-Cut Diamond Instruments (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code HNN (Knife, Ophthalmic). 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 Fine-Cut Diamond Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fine-Cut Diamond Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fine-Cut Diamond 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 “Fine-Cut”

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

Fine-Tune 4 Fine Optics, Inc. 2 Fine Surgical Instrument Corp. 1 Fine Spring Ent. Co., Ltd. 1 Fine Advanced Compound Co., Ltd. 1

Fine-Cut Diamond Instruments

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Fine-Cut”