Vilex, LLC - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Vilex, LLC has 16 FDA 510(k) cleared orthopedic devices. Based in Mcminnville, US.
Latest FDA clearance: Mar 2025. Active since 2020.
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) cleared devices by Vilex, LLC
16 devices
Cleared
Mar 05, 2025
TITANEX Screw Systems
Orthopedic
30d
Cleared
Dec 02, 2024
Hintermann Series H2 Total Ankle System
Orthopedic
286d
Cleared
Nov 27, 2024
TACTIX Vector Syndesmosis System
Orthopedic
26d
Cleared
Aug 28, 2024
REDEMPTION Charcot Plating System
Orthopedic
272d
Cleared
Aug 01, 2024
TACTIX Vector Syndesmosis System
Orthopedic
210d
Cleared
Jan 30, 2024
Redemption Duo Hindfoot Nail System
Orthopedic
266d
Cleared
Sep 11, 2023
TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System
Orthopedic
110d
Cleared
Aug 11, 2023
NITINEX Memory Compression Staple
Orthopedic
80d
Cleared
Jul 17, 2023
OPTIX H2 Patient Specific Instrument System
Orthopedic
146d
Cleared
Apr 25, 2023
ALPHALOK Plating System
Orthopedic
90d
Cleared
Dec 13, 2022
REDEMPTION Beaming System
Orthopedic
218d
Cleared
Nov 15, 2022
ALPHALOK Plating System
Orthopedic
168d