510(k) Report

FDA applicant

Antyllos Medizintechnik GmbH

Wurmlingen, DE1 decision2001–20010 recalls

FDA records 1 decision for Antyllos Medizintechnik GmbH (Wurmlingen, DE) in 2001: 1 510(k) clearance. All are in product code GEI (Electrosurgical, Cutting & Coagulation &…). 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 Antyllos Medizintechnik GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Antyllos Medizintechnik GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Antyllos Medizintechnik GmbH 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?

  • GEIElectrosurgical, Cutting & Coagulation & Accessories1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K010192Endoscopic Tube Shaft Instruments for Monoplar CoagulationAntyllos Medizintechnik GmbH · 20011cites it

What has FDA decided for it lately?

  • K010192Endoscopic Tube Shaft Instruments for Monoplar CoagulationAntyllos Medizintechnik GmbH · 2001

The one decision as Antyllos Medizintechnik GmbH →