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.

Claronav, Inc.

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

Total Devices4
Categories2
Latest Approval2024-07-25
TypeNumberDevice NameCodeDate
510(k) K233563 Navident PLV 2024-07-25 View
510(k) K210947 Navident PLV 2022-06-27 View
510(k) K163439 NaviENT HAW 2017-09-01 View
510(k) K161406 Navident PLV 2016-09-08 View