Identity
- Trade Name
- Vilex Fibula Nail FDA UDI
- Generic Name
- Arthrodesis nail, non-sterile FDA UDI
- Device Name
- Screw, Fibula Nail 2.7x24mm Ti L. Blue FDA UDI
- Model / Reference
- FXS27-24T FDA UDI
- Description
- Screw, Fibula Nail 2.7x24mm Ti L. Blue FDA UDI
Identifiers
- Catalog Number
- FXS27-24T FDA UDI
- Primary DI / UDI-DI
- 00841731119438 FDA UDI
- 510(k) Number
- K151456 FDA UDI
- FDA Product Code
- HSB FDA UDI
- GMDN Term
- Arthrodesis nail, non-sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3020 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Arthrodesis nail, non-sterile
Vilex Fibula Nail by Vilex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Arthrodesis nail, non-sterile.
- NEONAIL — Neoortho Produtos Ortopédicos S/A. · Class II
- NEONAIL — Neoortho Produtos Ortopédicos S/A. · Class II
- NEONAIL — Neoortho Produtos Ortopédicos S/A. · Class II
- ENDER NAIL — Smith & Nephew, Inc. · Class II
- NEONAIL — Neoortho Produtos Ortopédicos S/A. · Class II
- NEONAIL — Neoortho Produtos Ortopédicos S/A. · Class II
- NEONAIL — Neoortho Produtos Ortopédicos S/A. · Class II
- NEONAIL — Neoortho Produtos Ortopédicos S/A. · Class II
Cleared under the same submission
K151456 also covers:
- Fibula Nail — Vilex, Inc.
- Fibula Nail — Vilex, Inc.
- Vilex Fibula Drill — Vilex, Inc.
- Vilex Fibula Drill — Vilex, Inc.
- Vilex Fibula Nail — Vilex, Inc.
- Vilex Fibula Nail — Vilex, Inc.
- Vilex Fibula Nail — Vilex, Inc.
- Vilex Fibula Nail — Vilex, Inc.
- Vilex Fibula Nail — Vilex, Inc.
- Vilex Fibula Nail — Vilex, Inc.
- Vilex Fibula Nail — Vilex, Inc.
- Vilex Fibula Nail — Vilex, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Vilex, Inc.
Sources (1)
- FDA UDI 7be05da8-1cd1-4ed3-96be-a033ee6321e6 35 fields · synced May 30, 2026