510(k) K120089 ยท DZE Implant, Endosseous, Root-Form
BIOGENESIS IMPLANT SYSTEM
| Applicant | Biogenesis Co., Ltd., Anaheim CA, US |
| Decision | Substantially Equivalent, Mar 13, 2013 |
| Received | Jan 11, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120089
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.