510(k) K052369 ยท DZE Implant, Endosseous, Root-Form
EXFEEL IMPLANT SYSTEM
| Applicant | Megagen Co., Ltd., Santa Fe Springs CA, US |
| Decision | Substantially Equivalent, Jan 10, 2006 |
| Received | Aug 29, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052369
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.