510(k) Report

FDA applicant

S & T AG

Lake Forest, IL2 decisions2002–20030 recalls

FDA records 2 decisions for S & T AG (Lake Forest, IL) from 2002 to 2003: 2 510(k) clearances. Most are in product codes GAR (Suture, Nonabsorbable, Synthetic, Polyamide) and DXC (Clamp, Vascular). 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 & T AG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for S & T AG since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — S & T AG 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?

  • GARSuture, Nonabsorbable, Synthetic, Polyamide1decision
  • DXCClamp, Vascular1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K022754S&T Single Use Micro Anastomosis ClampS & T AG · 20022cite it
  • K031531S&T Microsurgical SutureS & T AG · 20031cites it

What has FDA decided for it lately?

  • K031531S&T Microsurgical SutureS & T AG · 2003
  • K022754S&T Single Use Micro Anastomosis ClampS & T AG · 2002

All 2 as S & T AG →