510(k) Report

FDA applicant

Far East Intl. Trading Corp.

Los Angeles, CA2 decisions1988–19880 recalls

FDA records 2 decisions for Far East Intl. Trading Corp. (Los Angeles, CA) in 1988: 2 510(k) clearances. Most are in product codes GES (Blade, Scalpel) and HRQ (Hemostat). 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 Far East Intl. Trading Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Far East Intl. Trading Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Far East Intl. Trading Corp. 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?

  • GESBlade, Scalpel1decision
  • HRQHemostat1decision

What has FDA decided for it lately?

  • K881638Surgical BladeFar East Intl. Trading Corp. · 1988
  • K881937Surgical InstrumentsFar East Intl. Trading Corp. · 1988

All 2 as Far East Intl. Trading Corp. →