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

Proprio, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories1
Latest FDA decision2025-12-15
TypeNumberDevice NameCodeDateActions
510(k) K252950 Paradigm SystemOLO2025-12-15 View
510(k) K250879 Paradigm SystemOLO2025-06-04 View
510(k) K243258 Paradigm SystemOLO2025-02-21 View
510(k) K222291 Paradigm SystemOLO2023-04-21 View

Related Clinical Trials