FDA applicant
Imcor
FDA records 7 decisions for Imcor (Edina, MN) from 1996 to 1999: 7 510(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 Imcor’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Imcor since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Imcor’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