510(k) K253365 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
LuxCreo Flexible Partial Denture Resin
| Applicant | LuxCreo, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Nov 25, 2025 |
| Received | Sep 30, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253365
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.