Medical Device Manufacturer · US , Pleasant Hills , PA

Vilex, Inc. - FDA 510(k) Cleared Devices

13 submissions · 12 cleared · Since 1998

Total

Cleared

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

1-13 of 13

Cleared Jul 23, 2014

VILEX ULTIMA EXTERNAL FIXATION SYSTEM WITH HA COATED PINS AND WIRES

K132820 · JDW

Orthopedic · 317d

Cleared Oct 09, 2012

VILEX EZ-STAPLE (MEMORY BONE FIXATION STAPLE)

K112837 · JDR

Orthopedic · 377d

Cleared Nov 14, 2011

FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL

MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION

VILEX BONE PLATE SYSTEM

CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675,...

K023684 · KWD

Orthopedic · 486d

Cleared Mar 18, 2002

VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09

K014154 · HWC

Orthopedic · 90d

Cleared Apr 26, 1999

VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, ORTHEX CANNULATED...

K991151 · HWC

Orthopedic · 20d

Cleared Apr 26, 1999

VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW, MODELS P222-XX, S25-XX, P227-XX,...

K991197 · HWC

Orthopedic · 19d

Cleared Jan 16, 1998

VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW

K973309 · HWC

Orthopedic · 135d

Vilex, Inc. - FDA 510(k) Cleared Devices

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