510(k) K212702 ยท DZE Implant, Endosseous, Root-Form
IM/ST Fixture System
| Applicant | Guilin Fiteeth Medical Instrument Co., Ltd., Guilin, CN |
| Decision | Substantially Equivalent, Oct 13, 2022 |
| Received | Aug 26, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212702
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.