Vilex, Inc.
Vilex, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2014.
Top product codes for Vilex, Inc.
Recent clearances by Vilex, Inc.
- K132820 — VILEX ULTIMA EXTERNAL FIXATION SYSTEM WITH HA COATED PINS AND WIRES
- K112837 — VILEX EZ-STAPLE (MEMORY BONE FIXATION STAPLE)
- K102413 — FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL
- K102401 — HEMI IMPLANT; MINI HEMI IMPLANT
- K070052 — MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION
- K052196 — VILEX X-FIX
- K041287 — VILEX BONE PLATE SYSTEM
- K041289 — TALUS OF VILEX (TOV)
- K023684 — CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365
- K014154 — VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00
- K991151 — VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, ORTHEX CANNULATED BONE SCREW
- 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
- K973309 — VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW
Data sourced from openFDA. This site is unofficial and independent of the FDA.