Mentor Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
61
Inspections
0
Compliance Actions
0

Known Names

mentor, mentor worldwide, mentor o and o

Recent 510(k) Clearances

K-NumberDeviceDate
K130813MENTOR CPX 4 BREAST TISSUE EXPANDERS AND MENTOR CPX 4 WITH SUTURE TABS BREAST TISSUE EXPANDERSApril 11, 2013
K053414MENTOR NOVASILK MESHDecember 27, 2005
K050008MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETERJune 3, 2005
K042851MENTOR OBTAPE TRANS-OBTURATOR SURGICAL KITNovember 9, 2004
K040959MENTOR GENESIS PENILE PROSTHESISOctober 29, 2004
K031767MENTOR OBTAPE TRANS-OBTURATOR TAPEJuly 17, 2003
K011493MENTOR ISOLOADER AUTOMATIC NEEDLE LOADING SYSTEM AND PHYSICS WORKSTATION FOR BRACHYTHERAPYOctober 1, 2002
K011500MENTOR CONTOUR PROFILE TISSUE EXPANDERDecember 3, 2001
K004005MENTOR ULTRASOUND-ASSISTED TISSUE REMOVAL SYSTEM (CURRENT), MENTOR CONTOUR GENESIS SYSTEM (PROPOSED)October 12, 2001
K010709MENTOR STERILE SALINE MAMMARY VOLUME SIZERSApril 23, 2001
K003873MENTOR SELF-CATH CLOSED SYSTEMMarch 29, 2001
K003784MENTOR SELF-CATH PLUSMarch 5, 2001
K993308MENTOR EVACARE VAGINAL PESSARIESDecember 13, 1999
K983065MENTOR ULTRASOUND-ASSISTED TISSUE REMOVAL SYSTEMDecember 1, 1998
K981527MENTOR PATHWAY INTRODUCER/DILATORJuly 9, 1998
K980483MENTOR SUSPEND SLINGApril 30, 1998
K980050MENTOR SKIN PROTECTION PADFebruary 27, 1998
K974469MENTOR PHACOEMULSIFICATION SISTEM REMOTE CONTROLFebruary 24, 1998
K970471MENTOR ULTRASOUND ASSISTED TISSUE REMOVAL SYSTEM (TRS)July 17, 1997
K963066MENTOR INJECTION PORT DETECTOR (IPD)September 27, 1996