Organogenesis, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Organogenesis, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Canton, US.
Last cleared in 2023. Active since 1997.
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 Organogenesis, Inc.
12 devices
Cleared
May 02, 2023
FortiShield (Biosynthetic Wound Matrix)
General & Plastic Surgery
624d
Cleared
Jul 01, 2022
PuraPly Micronized Wound Matrix (PuraPly MZ)
General & Plastic Surgery
148d
Cleared
Aug 30, 2007
FORTAGEN ORAL MEMBRANE
Dental
84d
Cleared
Nov 08, 2005
FORTADERM ANTIMICROBIAL WOUND DRESSING
General & Plastic Surgery
140d
Cleared
Nov 02, 2004
CUFFPATCH
General & Plastic Surgery
21d
Cleared
May 15, 2002
FORTAFLEX SURGICAL SLING
General & Plastic Surgery
40d
Cleared
May 10, 2002
FORTAFLEX SURGICAL MESH
General & Plastic Surgery
35d
Cleared
Mar 18, 2002
FORTAFLEX SURGICAL MESH
General & Plastic Surgery
70d
Cleared
Aug 24, 2001
FORTAFLEX SURGICAL MESH
General & Plastic Surgery
141d
Cleared
Jun 13, 2001
FORTADERM WOUND DRESSING
General & Plastic Surgery
70d
Cleared
May 30, 2001
FORTAFLEX SURGICAL SLING
General & Plastic Surgery
55d
Cleared
Aug 01, 1997
GRAFT PATCH
General & Plastic Surgery
169d