510(k) Report

FDA applicant

Industrielle Entwicklung Medizintechnik Und Vertri

Bonita Springs, FL2 decisions1999–20000 recalls

FDA records 2 decisions for Industrielle Entwicklung Medizintechnik Und Vertri (Bonita Springs, FL) from 1999 to 2000: 2 510(k) clearances. Most are in product codes DXQ (Blood Pressure Cuff) and DXN (System, Measurement, Blood-Pressure…). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, cardiovascular panel, where it files most

How often FDA has decided Industrielle Entwicklung Medizintechnik Und Vertri’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Industrielle Entwicklung Medizintechnik Und Vertri since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Industrielle Entwicklung Medizintechnik Und Vertri by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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