510(k) K103537 ยท DZE Implant, Endosseous, Root-Form
ET III SA ULTRA WIDE SYSTEM
| Applicant | Hiossen, Inc., Fariless Hills PA, US |
| Decision | Substantially Equivalent, Mar 10, 2011 |
| Received | Dec 2, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103537
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.