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.

Citieffe S.R.L.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories3
Latest Approval2025-10-17
TypeNumberDevice NameCodeDate
510(k) K250197 Estremo Fibular Nail HSB 2025-10-17 View
510(k) K183666 EBA One Nailing System HSB 2019-11-14 View
510(k) K181540 Estremo Citieffe Nailing System HSB 2019-01-16 View
510(k) K180150 PL8 Wrist Reconstruction Plate HRS 2018-08-02 View
510(k) K163323 Dolphix® External Fixation System MR Conditional KTT 2017-03-20 View