510(k) K261312 · MLP Keratoprosthesis, Temporary Implant, Surgical Use
Temporary Keratoprosthesis (QuickSet TKP)
| Applicant | Eyekon Medical, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Jul 24, 2026 |
| Received | Apr 21, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261312
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.