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Orthosonics, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K093805OSCAR 3February 19, 2010
K083830OSCAR BONE RESECTORMarch 20, 2009
K051053OSCAR, MODEL OE3000DBJuly 21, 2005
K021502OSCAR, MODEL OE3000June 6, 2002