Vilex, Inc.

13 FDA 510(k) medical device clearances.

Top product codes for Vilex, Inc.

Recent clearances by Vilex, Inc.

K132820 — VILEX ULTIMA EXTERNAL FIXATION SYSTEM WITH HA COATED PINS AND WIRES JDW · 2014-07-23
K112837 — VILEX EZ-STAPLE (MEMORY BONE FIXATION STAPLE) JDR · 2012-10-09
K102413 — FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL HSB · 2011-11-14
K102401 — HEMI IMPLANT; MINI HEMI IMPLANT KWD · 2011-07-20
K070052 — MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION KWD · 2007-03-28
K052196 — VILEX X-FIX KTT · 2005-11-22
K041287 — VILEX BONE PLATE SYSTEM HWC · 2004-08-05
K041289 — TALUS OF VILEX (TOV) HWC · 2004-08-05
K023684 — CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365 KWD · 2004-03-01
K014154 — VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00 HWC · 2002-03-18
K991151 — VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, ORTHEX CANNULATED BONE SCREW HWC · 1999-04-26
K991197 — VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW, MODELS P222-XX, S25-XX, P227-XX, S30-XX, P235-XX, S35-XX, P240-XX, S40-XX, P24 HWC · 1999-04-26
K973309 — VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW HWC · 1998-01-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.