Vivoxid , Ltd.

FDA Regulatory Profile

Vivoxid , Ltd. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 1, 2008.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K071199BONALIVE GRANULESFebruary 1, 2008
K071937BONALIVE GRANULES AND BONALIVE PLATESOctober 19, 2007
K070055BONALIVE GRANULES AND BONALIVE PLATESJune 25, 2007