510(k) Report

FDA applicant

Miele Professional

Somerset, NJ1 decision1996–19960 recalls

FDA records 1 decision for Miele Professional (Somerset, NJ) in 1996: 1 510(k) clearance. All are in product code LDS (Device, Pasteurization, Hot Water). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Miele Professional since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Miele Professional 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?

  • LDSDevice, Pasteurization, Hot Water1decision

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.

  • K950518Miele G 7781 Dental Thermal DisinfectorMiele Professional · 19961cites it

What has FDA decided for it lately?

  • K950518Miele G 7781 Dental Thermal DisinfectorMiele Professional · 1996

The one decision as Miele Professional →

Other applicant names beginning “Miele”

FDA records each applicant name separately; these may or may not be the same firm.

Miele, Inc. 1Miele Appliances, Inc. 1