510(k) Report

FDA applicant

Hmt High Medical Technologies AG

Washington, DC1 decision2004–20040 recalls

FDA records 1 decision for Hmt High Medical Technologies AG (Washington, DC) in 2004: 1 510(k) clearance. All are in product code LNS (Lithotriptor, Extracorporeal Shock-Wave…). 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 Hmt High Medical Technologies AG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hmt High Medical Technologies AG since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hmt High Medical Technologies 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?

  • LNSLithotriptor, Extracorporeal Shock-Wave, Urological1decision

What has FDA decided for it lately?

  • K040741Ultrasound Localization System Uls 0142Hmt High Medical Technologies AG · 2004

The one decision as Hmt High Medical Technologies AG →