Mentor Corp. - FDA 510(k) Cleared Devices
Recent clearances: MENTOR CPX 4 BREAST TISSUE EXPANDERS AND MENTOR CPX 4 WITH SUTURE TABS BREAST TISSUE EXPANDERS, MENTOR NOVASILK MESH, MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETER
61
Total
61
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mentor Corp. General & Plastic Surgery ✕
20 devices
Cleared
Apr 11, 2013
MENTOR CPX 4 BREAST TISSUE EXPANDERS AND MENTOR CPX 4 WITH SUTURE TABS BREAST...
General & Plastic Surgery
17d
Cleared
Dec 03, 2001
MENTOR CONTOUR PROFILE TISSUE EXPANDER
General & Plastic Surgery
201d
Cleared
Oct 12, 2001
MENTOR ULTRASOUND-ASSISTED TISSUE REMOVAL SYSTEM (CURRENT), MENTOR CONTOUR...
General & Plastic Surgery
290d
Cleared
Apr 23, 2001
MENTOR STERILE SALINE MAMMARY VOLUME SIZERS
General & Plastic Surgery
45d
Cleared
Dec 01, 1998
MENTOR ULTRASOUND-ASSISTED TISSUE REMOVAL SYSTEM
General & Plastic Surgery
90d
Cleared
Jul 09, 1998
MENTOR PATHWAY INTRODUCER/DILATOR
General & Plastic Surgery
72d
Cleared
Apr 30, 1998
MENTOR SUSPEND SLING
General & Plastic Surgery
80d
Cleared
Feb 27, 1998
MENTOR SKIN PROTECTION PAD
General & Plastic Surgery
52d
Cleared
Jul 17, 1997
MENTOR ULTRASOUND ASSISTED TISSUE REMOVAL SYSTEM (TRS)
General & Plastic Surgery
160d
Cleared
Sep 27, 1996
MENTOR INJECTION PORT DETECTOR (IPD)
General & Plastic Surgery
51d
Cleared
Aug 22, 1996
MENTOR H/S SILICONE GEL SHEETING FOR SCAR MANAGEMENT
General & Plastic Surgery
91d
Cleared
Feb 11, 1991
ACCU-TEC SYSTEM FOR TISSUE EXPANDER INJECTION PORT
General & Plastic Surgery
67d