FDA applicant

A. Titan Instruments, Inc.

Hamburg, NY1 decision2006–20060 recalls

FDA records 1 decision for A. Titan Instruments, Inc. (Hamburg, NY) in 2006: 1 510(k) clearance. All are in product code EMG (Forceps, Tooth Extractor, Surgical). 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, dental panel, where it files most

How often FDA has decided A. Titan Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for A. Titan Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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A. Titan Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?