Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Uroviu Corporation with 7 510(k) clearances. The most recent is a 510(k) clearance dated Oct 23, 2025: UV5000W Handle.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Oct 23, 2025 | UV5000W HandleK253226 · FAJ | 510(k) clearances |
| Sep 11, 2025 | UV5000 HandleK250797 · FAJ | 510(k) clearances |
| Dec 13, 2024 | Uro-G HD Cystoscope (1520)K243196 · FAJ | 510(k) clearances |
| Jun 7, 2024 | Uro-G HD Flexible CystoscopeK232837 · FAJ | 510(k) clearances |
| May 4, 2021 | Uro-G CystoscopeK202921 · FAJ | 510(k) clearances |
| Jul 2, 2019 | Uro-N CystoscopeK182876 · FAJ | 510(k) clearances |
| Jan 30, 2018 | Uro-V CystoscopeK171500 · FAJ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
