510(k) K221678 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
SprintRay High Impact Denture Base
| Applicant | Sprintray, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Nov 10, 2022 |
| Received | Jun 9, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221678
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.