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.

Phenox, Ltd.

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

Total Devices3
Categories2
Latest FDA decision2026-01-15
TypeNumberDevice NameCodeDateActions
510(k) K251357 Esperance pHLO Aspiration SystemNRY2026-01-15 View
510(k) K242420 pNOVUS 21 MicrocatheterDQO2024-11-12 View
510(k) K221279 pNOVUS 21 MicrocatheterDQO2022-11-28 View

Related Clinical Trials

NCT07143019The Use of p48/64 MW HPC Flow Modulation Device in the Treatment of Wide-necked Intracranial AneurysmsRECRUITINGNCT07748572PMCF Registry to Describe the Safety and Performance of p64, p48 MW and p64 MW in FranceRECRUITINGNCT07757113Comparative Study of Embolic Agents in Patients With Subdural Hemorrhage Undergoing Middle Meningeal Artery (MMA) EmbolizationNOT_YET_RECRUITING
↑