510(k) K100100 ยท DZE Implant, Endosseous, Root-Form
DIO STEADY EXTERNAL IMPLANT SYSTEM
| Applicant | Dio Corporation, Los Angeles CA, US |
| Decision | Substantially Equivalent, Nov 10, 2010 |
| Received | Jan 12, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100100
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.