510(k) Report

FDA applicant

Erchinger Medizintecnik

Amsterdam, NL1 decision2000–20000 recalls

FDA records 1 decision for Erchinger Medizintecnik (Amsterdam, NL) in 2000: 1 510(k) clearance. All are in product code FHN (Ligator, Hemorrhoidal). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Erchinger Medizintecnik’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Erchinger Medizintecnik since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Erchinger Medizintecnik 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?

  • FHNLigator, Hemorrhoidal1decision

Who builds on its devices?

Later devices cite its devices 2 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.

  • K000297Erchinger Hemorrhoidal Ligators: Suction Ligators, Mod. Erchinger, Rudd, Mcgivney Mod. ErchingerErchinger Medizintecnik · 20002cite it

What has FDA decided for it lately?

  • K000297Erchinger Hemorrhoidal Ligators: Suction Ligators, Mod. Erchinger, Rudd, Mcgivney Mod. ErchingerErchinger Medizintecnik · 2000

The one decision as Erchinger Medizintecnik →