Mentor Corporation

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K062421MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZEROctober 10, 2006
K053296MENTOR ARIS SUPRAPUBIC SURGICAL KITDecember 15, 2005
K052440MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETEROctober 11, 2005
K050148MENTOR ARIS TRANS-OBTURATOR TAPE AND SURGICAL KITMarch 9, 2005