FDA applicant

Zinnanti Surgical Instruments, Inc.

Chatsworth, CA76 decisions1984–19970 recalls

FDA records 76 decisions for Zinnanti Surgical Instruments, Inc. (Chatsworth, CA) from 1984 to 1997: 76 510(k) clearances. Most are in product codes KNA (Instrument, Manual, Specialized…) and LRW (Scissors, General, 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Zinnanti Surgical Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Zinnanti Surgical Instruments, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?