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Sign in to claim this brandVilex, Inc.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 111 MOFFITT ST, MCMINNVILLE, TN, 37110
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1051526
- DUNS Number
- —
Catalogue (2304)
Page 46 of 47| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vilex Dual Thread Screw | F50-50T-20XS | FDA UDI | Class II | Active |
| Vilex Lag Screw | S45-38T-16 | FDA UDI | Class II | Active |
| Vilex Lag Screw | S35-20T-11 | FDA UDI | Class II | Active |
| Vilex Plate Screw | PS35-16T | FDA UDI | Class II | Active |
| Vilex Lag Screw, FT | FT30-20S-11 | FDA UDI | Class II | Active |
| Vilex Lag Screw | S25-08T-09 | FDA UDI | Class II | Active |
| Fuze | FTZ50-20TH | FDA UDI | Class II | Active |
| Vilex Dual Thread Screw | F20-32T-09 | FDA UDI | Class II | Active |
| Vilex Plate Screw | PS30-14T | FDA UDI | Class II | Active |
| Vilex AVID Plate Screw | ASN42-18T | FDA UDI | Class II | Active |
| Vilex Jones Fracture | JF55-70T-18 | FDA UDI | Class II | Active |
| Vilex AVID Plate Screw | ASL42-38T | FDA UDI | Class II | Active |
| Vilex Dual Thread Screw | F50-115T-20 | FDA UDI | Class II | Active |
| Vilex Lag Screw | S25-20T-09 | FDA UDI | Class II | Active |
| Vilex Jones Fracture | JF60-52T | FDA UDI | Class II | Active |
| Vilex Lag Screw | S35-12T-11 | FDA UDI | Class II | Active |
| Vilex Lag Screw | S35-46S-11 | FDA UDI | Class II | Active |
| Vilex Dual Thread Screw | F50-80T-20XS | FDA UDI | Class II | Active |
| Vilex Jones Fracture Guidewire | K200-18S | FDA UDI | Class I | Active |
| Vilex Dual Thread Screw | F20-25T-09 | FDA UDI | Class II | Active |
| Vilex Jones Fracture | JF55-68T-18 | FDA UDI | Class II | Active |
| Vilex AVID Plate Screw | ASL35-36T | FDA UDI | Class II | Active |
| Vilex Dual Thread Screw | F50-40T-20XS | FDA UDI | Class II | Active |
| Vilex Lag Screw | S65-80S-20 | FDA UDI | Class II | Active |
| TITANEX Screw Systems | K250304 | FDA 510(k) | Class II | Active |
| Vilex/Duval/Orthex Cannulated Bone Screw, Models P222-Xx, S25-Xx, P227-Xx, S30-Xx, P235-Xx, S35-Xx, P240-Xx, S40-Xx, P24 | K991197 | FDA 510(k) | Class II | Active |
| Vilex Ultima External Fixation System With Ha Coated Pins And Wires | K132820 | FDA 510(k) | Class II | Active |
| Correx Software | K212552 | FDA 510(k) | Class II | Active |
| ALPHALOK Plating System | K230204 | FDA 510(k) | Class II | Active |
| Dynex Ring Fixation System, Diametrix Ring Fixation System | K202054 | FDA 510(k) | Class II | Active |
| ALPHALOK Plating System | K221558 | FDA 510(k) | Class II | Active |
| DYNEX® External Fixation Systems | K260900 | FDA 510(k) | Class II | Active |
| Dynex Micro | K202143 | FDA 510(k) | Class II | Active |
| Vilex Cannulated Bone Screw, Duval Cannulated Bone Screw | K973309 | FDA 510(k) | Class II | Active |
| Hemi Implant; Mini Hemi Implant | K102401 | FDA 510(k) | Class II | Active |
| ALPHALOK™ Plating System | K212348 | FDA 510(k) | Class II | Active |
| Vilex Cannulated Bone Screw, Duval Cannulated Bone Screw, Orthex Cannulated Bone Screw | K991151 | FDA 510(k) | Class II | Active |
| TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System | K231504 | FDA 510(k) | Class II | Active |
| NITINEX Memory Compression Staple | K231493 | FDA 510(k) | Class II | Active |
| REDEMPTION Charcot Plating System | K233816 | FDA 510(k) | Class II | Active |
| Vilex X-Fix | K052196 | FDA 510(k) | Class II | Active |
| Cannulated Metallic Hemi Toe Implant, Models Mpj241975, Mpj221775, Mpj211675, Mpj191565, Mpj171365 | K023684 | FDA 510(k) | Class II | Active |
| Fuze: Intramedullary Internal Fixation Nail | K102413 | FDA 510(k) | Class II | Active |
| Redemption Duo Hindfoot Nail System | K231343 | FDA 510(k) | Class II | Active |
| Vilex Bone Plate System | K041287 | FDA 510(k) | Class II | Active |
| Vilex Ez-Staple (memory Bone Fixation Staple) | K112837 | FDA 510(k) | Class II | Active |
| OPTIX H2 Patient Specific Instrument System | K230462 | FDA 510(k) | Class II | Active |
| Talus Of Vilex (tov) | K041289 | FDA 510(k)FDA UDI | Class II | Active |
| REDEMPTION Beaming System | K221342 | FDA 510(k)FDA UDI | Class II | Active |
| TACTIX Vector Syndesmosis System | K243408 | FDA 510(k) | Class II | Active |
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