510(k) K261802 · EBI Resin, Denture, Relining, Repairing, Rebasing
Glidewell Denture Base Resin
| Applicant | Prismatik Dentalcraft, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Aug 27, 2026 |
| Received | Jun 1, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261802
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.