510(k) K181331 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
JUVORA Oyster White Dental Disc, CERAMILL PEEK by JUVORA, Oyster White
| Applicant | Juvora, Ltd., Thornton-Clevelys, GB |
| Decision | Substantially Equivalent, Dec 21, 2018 |
| Received | May 21, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181331
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.