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.

Reprobitech Corp.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest Approval2018-02-09
TypeNumberDevice NameCodeDate
510(k) K172751 iVitri Straw MQK 2018-02-09 View
510(k) K162640 iVitri EZ MQK 2017-06-30 View