510(k) K260708 ยท FGB Ureteroscope And Accessories, Flexible/Rigid
Vein360 Reprocessed LithoVue Digital Flexible Ureteroscope (Standard Deflection); Vein360 Reprocessed LithoVue Digital Flexible Ureteroscope (Reverse Deflection)
| Applicant | Vein 360, Cincinnati OH, US |
| Decision | Substantially Equivalent, Oct 20, 2026 |
| Received | Mar 4, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260708
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.