510(k) K203701 ยท DZE Implant, Endosseous, Root-Form
Locator Overdenture Implant System
| Applicant | Ivory Super Holdco Inc. / Zest Anchors, LLC, Carlsbad CA, US |
| Decision | Substantially Equivalent, Apr 15, 2021 |
| Received | Dec 18, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203701
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.