Mentor Worldwide, LLC - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Mentor Worldwide, LLC has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Santa Barbara, US.
Latest FDA clearance: Apr 2025. Active since 2013.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mentor Worldwide, LLC
12 devices
Cleared
Apr 24, 2025
MENTOR™ PliaForm™ Breast Tissue Expander w/ Suture Tabs
General & Plastic Surgery
211d
Cleared
Jan 13, 2025
MENTOR™ MemoryShape™ Resterilizable Gel Breast Implant Sizer
General & Plastic Surgery
89d
Cleared
Jan 12, 2025
Mentor™ CPX ™ 4 PLUS Enhance Breast Tissue Expander
General & Plastic Surgery
30d
Cleared
Sep 06, 2024
MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer
General & Plastic Surgery
98d
Cleared
Aug 02, 2024
MENTOR™ CPX™4 PLUS Enhance Breast Tissue Expander
General & Plastic Surgery
32d
Cleared
Sep 25, 2018
CPX 4 Breast Tissue Expander with Smooth Surface
General & Plastic Surgery
28d
Cleared
May 23, 2016
ARTOURA Breast Tissue Expanders with Smooth Surface
General & Plastic Surgery
27d
Cleared
Feb 19, 2016
CPX 4 Breast Tissue Expander
General & Plastic Surgery
171d
Cleared
May 20, 2015
Mentor MemoryShape Resterilizable Gel Breast Implant Sizer STERILE
General & Plastic Surgery
30d
Cleared
Apr 24, 2015
Artoura Breast Tissue Expander
General & Plastic Surgery
30d
Cleared
Dec 19, 2014
CPX Control Breast Tissue Expander
General & Plastic Surgery
63d
Cleared
Jul 17, 2013
MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZER
General & Plastic Surgery
26d