FDA applicant

Surgeon Surgical Instrumentation, Inc.

Placentia, CA10 decisions1983–19950 recalls

FDA records 10 decisions for Surgeon Surgical Instrumentation, Inc. (Placentia, CA) from 1983 to 1995: 10 510(k) clearances. Most are in product codes KYG (Device, Irrigation, Ocular Surgery) and GCT (Light Source, Endoscope, Xenon Arc). 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 Surgeon Surgical Instrumentation, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Surgeon Surgical Instrumentation, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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See the 510(k) Report

Other applicant names beginning “Surgeon”

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

The Surgeon General, Department of the Army 2 The Surgeon General, Department of the Army (TSG-DA) 2 Surgeon Design 1

Surgeon Surgical Instrumentation, 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?

Other applicant names beginning “Surgeon”