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Citieffe S.R.L.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250197Estremo Fibular NailOctober 17, 2025
K183666EBA One Nailing SystemNovember 14, 2019
K181540Estremo Citieffe Nailing SystemJanuary 16, 2019
K180150PL8 Wrist Reconstruction PlateAugust 2, 2018
K163323Dolphix® External Fixation System MR ConditionalMarch 20, 2017
K150661ST.A.R. 90 F4 External Fixation Screws With HydroxyapatiteJuly 7, 2015
K132363DOLPHIX EXTERNAL FIXATION SYSTEMJanuary 16, 2014
K131005EBA2 FEMORAL NAILING SYSTEMJune 25, 2013
K113388CITIEFFE-TITANIUM CANNULATED SCREWJune 5, 2012
K113384EXTERNAL FIXATOR ST.A R 90 F4May 1, 2012
K113387CITIEFFE TITANIUM NAILING SYSTEMMarch 15, 2012