510(k) K120198 ยท DZE Implant, Endosseous, Root-Form
LOCATOR OVERDENTURE IMPLANT SYSTEM
| Applicant | Zest Anchors, LLC, Escondido CA, US |
| Decision | Substantially Equivalent, Jun 6, 2012 |
| Received | Jan 23, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120198
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 22, 2019 | Zest Anchors LLC LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1 . Open, Classified |
DZE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.