Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Uro-1, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories2
Latest Approval2022-12-02
TypeNumberDevice NameCodeDate
510(k) K220611 SUREcore Plus Biopsy Instrument KNW 2022-12-02 View
510(k) K201650 VMCore Biopsy Needle KNW 2021-01-15 View
510(k) K180214 Repris Bladder Injection System FBK 2018-05-03 View