510(k) K220979 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
SprintRay Denture Base
| Applicant | Sprintray, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Sep 14, 2022 |
| Received | Apr 4, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220979
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.