FDA applicant
Industrielle Entwicklung Medizintechnik Und Vertri
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
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.
Planning a device like Industrielle Entwicklung…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report