510(k) K260006 ยท DZE Implant, Endosseous, Root-Form
INOSS System
| Applicant | Inosys, Inc., New York NY, US |
| Decision | Substantially Equivalent, Jun 17, 2026 |
| Received | Jan 2, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260006
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.