510(k) K093889 ยท DZE Implant, Endosseous, Root-Form
MODIFICATION TO: HG III ULTRA WIDE SYSTEM
| Applicant | Hiossen, Inc., Fariless Hills PA, US |
| Decision | Substantially Equivalent, Apr 22, 2010 |
| Received | Dec 18, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093889
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.