Prodeon Medical, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2026-06-22
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K261342 | Urocross Expander System (UES-2018-C1) | QKA | 2026-06-22 | View |
| 510(k) | K253525 | Urocross Expander System (Model Numbers ES2018 and ES3025) | QKA | 2026-03-12 | View |
| 510(k) | K252572 | Prodeon Urethral Sheath System | FED | 2025-10-07 | View |
No matching devices.