510(k) K160965 ยท DZE Implant, Endosseous, Root-Form
SuperLine
| Applicant | Dentium Co., Ltd., Seoul, KR |
| Decision | Substantially Equivalent, Jan 13, 2017 |
| Received | Apr 6, 2016 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K160965
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.