FDA applicant

A. Henniss

Tarzana, CA3 decisions1990–19910 recalls

FDA records 3 decisions for A. Henniss (Tarzana, CA) from 1990 to 1991: 3 510(k) clearances. Most are in product codes HBE (Drills, Burrs, Trephines & Accessories…) and GZT (Retractor, Self-Retaining, For Neurosurgery). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for A. Henniss since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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A. Henniss

Which product codes does it file in?

What has FDA decided for it lately?