Vilex, Inc. is one of 19082 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vilex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VILEX ULTIMA EXTERNAL FIXATION SYSTEM WITH HA COATED PINS AND WIRES, VILEX EZ-STAPLE (MEMORY BONE FIXATION STAPLE), FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL
13
Total
12
Cleared
0
Denied
Vilex, Inc. has 12 FDA 510(k) cleared orthopedic devices. Based in Pleasant Hills, US.
Historical record: 12 cleared submissions from 1998 to 2014.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vilex, Inc.
13 devices
Cleared
Jul 23, 2014
VILEX ULTIMA EXTERNAL FIXATION SYSTEM WITH HA COATED PINS AND WIRES
Orthopedic
317d
Cleared
Oct 09, 2012
VILEX EZ-STAPLE (MEMORY BONE FIXATION STAPLE)
Orthopedic
377d
Cleared
Nov 14, 2011
FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL
Orthopedic
447d
Cleared
Jul 20, 2011
HEMI IMPLANT
Orthopedic
330d
Cleared
Mar 28, 2007
MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION
Orthopedic
83d
Cleared
Nov 22, 2005
VILEX X-FIX
Orthopedic
103d
Cleared
Aug 05, 2004
VILEX BONE PLATE SYSTEM
Orthopedic
84d
Cleared
Aug 05, 2004
TALUS OF VILEX (TOV)
Orthopedic
84d
Cleared
Mar 01, 2004
CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675,...
Orthopedic
486d
Cleared
Mar 18, 2002
VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09
Orthopedic
90d
Cleared
Apr 26, 1999
VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, ORTHEX CANNULATED...
Orthopedic
20d
Cleared
Apr 26, 1999
VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW, MODELS P222-XX, S25-XX, P227-XX,...
Orthopedic
19d