510(k) K073486 ยท DZE Implant, Endosseous, Root-Form
DENTIS DENTAL IMPLANT SYSTEM
| Applicant | Dentis Co., Ltd., Santa Fe Springs CA, US |
| Decision | Substantially Equivalent, Apr 4, 2008 |
| Received | Dec 12, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073486
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.