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Vivoxid , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K071199
BONALIVE GRANULES
February 1, 2008
K071937
BONALIVE GRANULES AND BONALIVE PLATES
October 19, 2007
K070055
BONALIVE GRANULES AND BONALIVE PLATES
June 25, 2007