510(k) K153332 ยท DZE Implant, Endosseous, Root-Form
ETIII SA Fixture System (O3.2mm)
| Applicant | Hiossen, Inc., Fariless Hills PA, US |
| Decision | Substantially Equivalent, Oct 27, 2016 |
| Received | Nov 19, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153332
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.