Vilex, Inc.
United Statesfrom the FDA registration address FDA FEI 1051526
- Devices
- 3,307
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Vilex, Inc. makes
Vilex, Inc. manufactures orthopaedic devices including non-bioabsorbable bone screws and fixation plates, external orthopaedic fixation systems, ankle prosthesis bearings, surgical drill guides, tibia nails, and coated ankle tibia prostheses.
The company's devices are classified as Class I and Class II and are listed in the FDA UDI registry. Vilex, Inc. is based in the US.
Catalogue
Search and filter all 3,307 devicesShowing 1-50 of 3,307
Company details
- FDA FEI number
- 1051526
- Address
- 111 MOFFITT ST, MCMINNVILLE, TN, 37110
Frequently asked questions
How many devices does Vilex, Inc. have in the registry?
The registry currently lists 3307 devices for Vilex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vilex, Inc.'s devices?
Among its 50 most recently registered devices, Vilex, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Vilex, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Vilex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vilex, Inc. in the registry?
The most recently registered devices listed for Vilex, Inc. include REDEMPTION Beaming System RFT65-110T-24, REDEMPTION Beaming System RFT65-100T-24, REDEMPTION Beaming System RFT65-120T-24 and REDEMPTION Beaming System RFT65-115T-24.