Citieffe S.R.L.
Citieffe S.R.L. holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2025.
Top product codes for Citieffe S.R.L.
Recent clearances by Citieffe S.R.L.
- K250197 — Estremo Fibular Nail
- K183666 — EBA One Nailing System
- K181540 — Estremo Citieffe Nailing System
- K180150 — PL8 Wrist Reconstruction Plate
- K163323 — Dolphix® External Fixation System MR Conditional
- K150661 — ST.A.R. 90 F4 External Fixation Screws With Hydroxyapatite
- K132363 — DOLPHIX EXTERNAL FIXATION SYSTEM
- K131005 — EBA2 FEMORAL NAILING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.