Anulex Technologies, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Anulex Technologies, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Minnetonka, US.
Historical record: 12 cleared submissions from 2005 to 2012.
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.
12 devices
Cleared
Nov 09, 2012
MICRO/MINI N-PK(F) BONE ANCHOR
Orthopedic
189d
Cleared
Nov 09, 2012
MICRO/MINI N-PK(H) BONE ANCHOR
Orthopedic
189d
Cleared
Feb 23, 2012
FIXATE TISSUE BAND
General & Plastic Surgery
62d
Cleared
Dec 16, 2011
FIXATE TISSUE BAND
General & Plastic Surgery
29d
Cleared
Oct 27, 2011
FIXATE TISSUE BAND
General & Plastic Surgery
28d
Cleared
Sep 08, 2011
FIXATE TISSUE BAND
General & Plastic Surgery
105d
Cleared
Mar 17, 2010
VERSACLOSE, MODEL VC-200-01
General & Plastic Surgery
16d
Cleared
Jun 12, 2009
XCLOSE TISSUE REPAIR SYSTEM, MODEL XC-200-01
General & Plastic Surgery
29d
Cleared
Dec 19, 2008
RIMCLOSE BONE ANCHOR
Orthopedic
92d
Cleared
Sep 01, 2006
XCLOSE TISSUE REPAIR SYSTEM, MODEL SRS
General & Plastic Surgery
24d
Cleared
Jul 05, 2006
ANCHOR BAND SUTURING SYSTEM, MODEL SR-AB
General & Plastic Surgery
48d
Cleared
Aug 18, 2005
INCLOSE SURGICAL MESH SYSTEM
General & Plastic Surgery
122d