Vilex Inc

FDA Filings

This page includes the latest FDA filings for Vilex Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

FDA Filings

Device
Company
DeviceDate
VILEX, INC.
VILEX ULTIMA EXTERNAL FIXATION SYSTEM WITH HA COATED PINS AND WIRES2014-07-23
VILEX, INC.
VILEX EZ-STAPLE (MEMORY BONE FIXATION STAPLE)2012-10-09
VILEX, INC.
FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL2011-11-14
VILEX, INC.
HEMI IMPLANT; MINI HEMI IMPLANT2011-07-20
VILEX, INC.
MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION2007-03-28
VILEX, INC.
VILEX X-FIX2005-11-22
VILEX, INC.
TALUS OF VILEX (TOV)2004-08-05
VILEX, INC.
VILEX BONE PLATE SYSTEM2004-08-05
VILEX, INC.
CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ1713652004-03-01
VILEX, INC.
VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-002002-03-18
VILEX, INC.
VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW, MODELS P222-XX, S25-XX, P227-XX, S30-XX, P235-XX, S35-XX, P240-XX, S40-XX, P241999-04-26
VILEX, INC.
VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, ORTHEX CANNULATED BONE SCREW1999-04-26
VILEX, INC.
VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW1998-01-16

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