FDA applicant
Imz, GmbH
FDA records 12 decisions for Imz, GmbH (Potomac, MD) from 1995 to 1997: 12 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). 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 Imz, GmbH’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Imz, GmbH since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Imz, GmbH’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