510(k) K101096 ยท DZE Implant, Endosseous, Root-Form
HT III SA FIXTURE SYSTEM
| Applicant | Hiossen, Inc., Fariless Hills PA, US |
| Decision | Substantially Equivalent, Oct 8, 2010 |
| Received | Apr 20, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101096
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.