510(k) Report

FDA applicant

S. Cordero Co.

Mexico City Cp 01030, MX1 decision1986–19860 recalls

FDA records 1 decision for S. Cordero Co. (Mexico City Cp 01030, MX) in 1986: 1 510(k) clearance. All are in product code GDZ (Handle, Scalpel). 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, general and plastic surgery panel, where it files most

How often FDA has decided S. Cordero Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for S. Cordero Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • GDZHandle, Scalpel1decision

What has FDA decided for it lately?

  • K863808The S. Cordero StylusS. Cordero Co. · 1986

The one decision as S. Cordero Co. →