FDA applicant

Fine Surgical Instrument Corp.

Great Neck, NY1 decision2004–20040 recalls

FDA records 1 decision for Fine Surgical Instrument Corp. (Great Neck, NY) in 2004: 1 510(k) clearance. All are in product code HFX (Clamp, Circumcision). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Fine Surgical Instrument Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fine Surgical Instrument Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fine Surgical Instrument Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Fine Surgical Instrument Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Fine”

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

Fine-Tune 4 Fine Optics, Inc. 2 Fine Spring Ent. Co., Ltd. 1 Fine Advanced Compound Co., Ltd. 1 Fine-Cut Diamond Instruments 1

Fine Surgical Instrument Corp.

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 “Fine”