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Or-Nim Medical , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K150268
CerOX
November 6, 2015
K131854
CEROX
September 13, 2013
K100875
CEROX, MODEL 321OF
January 25, 2011
K093923
CEROX MODEL 3210
January 19, 2010
K073407
PACIFICA
February 28, 2008