Medical Device Manufacturer · US , Lakewood Ranch , FL

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

7 submissions · 7 cleared · Since 2014

Recent clearances: Bone Screw Line Addition, Cannulated Hemi Implant

7
Total
7
Cleared
0
Denied

Vilex IN Tennessee, Inc. has 7 FDA 510(k) cleared medical devices. Based in Lakewood Ranch, US.

Historical record: 7 cleared submissions from 2014 to 2019. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Vilex IN Tennessee, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vilex IN Tennessee, Inc.

7 devices
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