510(k) K123512 ยท DZE Implant, Endosseous, Root-Form
BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL D 3.0 TO 6.0 MM
| Applicant | Biodenta Swiss AG, Berneck, St.Gallen, CH |
| Decision | Substantially Equivalent, Mar 28, 2013 |
| Received | Nov 13, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123512
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.