Identity
- Trade Name
- VLP FDA UDI
- Generic Name
- Orthopaedic bone screw (non-sliding) FDA UDI
- Device Name
- VLP TITANIUM 2.0MM X 23MM CORTEX SCREW T6 SELF-TAPPING NON-STERILE FDA UDI
- Model / Reference
- 74402023N FDA UDI
- Description
- VLP TITANIUM 2.0MM X 23MM CORTEX SCREW T6 SELF-TAPPING NON-STERILE FDA UDI
Identifiers
- Catalog Number
- 74402023N FDA UDI
- Primary DI / UDI-DI
- 00885556383049 FDA UDI
- FDA Product Code
- HRS FDA UDI
- GMDN Term
- Orthopaedic bone screw (non-sliding) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
MR Conditional FDA UDI
Category: Orthopaedic bone screw (non-sliding)
Vlp by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic bone screw (non-sliding).
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Cleared under the same submission
K132886 also covers:
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- VLP — Smith & Nephew, Inc.
- VLP — Smith & Nephew, Inc.
- VLP — Smith & Nephew, Inc.
- VLP — Smith & Nephew, Inc.
- VLP — Smith & Nephew, Inc.
- VLP — Smith & Nephew, Inc.
- VLP — Smith & Nephew, Inc.
- VLP — Smith & Nephew, Inc.
- VLP — Smith & Nephew, Inc.
- VLP — Smith & Nephew, Inc.
K210837 also covers:
- CHS — Smith & Nephew, Inc.
- CHS — Smith & Nephew, Inc.
- D-RAD SMART PACK — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, 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
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI a0b5ade9-5b55-493d-a014-cb4c1e6388a4 36 fields · synced Jun 8, 2026