FDA applicant
Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz
FDA records 2 decisions for Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz (Tuttlingen, DE) from 1995 to 1997: 2 510(k) clearances. All are in product code HIF (Insufflator, Laparoscopic). 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 Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz since 2007.
Recalls per year
No recall linked to its devices since 2007.
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