510(k) K222142 ยท DZE Implant, Endosseous, Root-Form
BR SLA Type Implant System
| Applicant | Biotem Co., Ltd., Busan, KR |
| Decision | Substantially Equivalent, Jun 24, 2023 |
| Received | Jul 20, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222142
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.