510(k) K170732 ยท DZE Implant, Endosseous, Root-Form
Biomate Dental Implant System
| Applicant | Biomate Medical Devices Technology Co., Ltd., Kaohsiung City, TW |
| Decision | Substantially Equivalent, Oct 26, 2018 |
| Received | Mar 10, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170732
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.