510(k) Report

FDA applicant

MIPM Mammendorfer Institut für Physik und Medizin GmbH

Mammendorf, DE4 decisions2015–20250 recalls

FDA records 4 decisions for MIPM Mammendorfer Institut für Physik und Medizin GmbH (Mammendorf, DE) from 2015 to 2025: 4 510(k) clearances. Most are in product codes KOI (Stimulator, Nerve, Peripheral, Electric) and MWI (Monitor, Physiological, Patient (Without…). Its devices cite 4 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Mipm Mammendorfer Institut Fur Physik Und Medizin”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided MIPM Mammendorfer Institut für Physik und Medizin GmbH’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2015: 12016: 12022: 12025: 1
2015high 1 (2015) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — MIPM Mammendorfer Institut für Physik und Medizin GmbH by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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