510(k) K223814 ยท DZE Implant, Endosseous, Root-Form
Genesis ACTIVE Implant System
| Applicant | Keystone Dental, Inc., Burlington MA, US |
| Decision | Substantially Equivalent, May 25, 2023 |
| Received | Dec 20, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223814
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.