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Innovia, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K093783INNOVIA INNOPORT LAPAROSCOPIC ACCESS PORTAugust 23, 2010
K090677INNOPORT LAPAROSCOPIC ACCESS DEVICEMay 7, 2009
K060151ORBITAL TISSUE EXPANDER (OTE)August 8, 2006