Identity
- Trade Name
- RENOVOLIFE LLC FDA UDI
- Generic Name
- Tibia nail, non-sterile FDA UDI
- Device Name
- Intramedullary Fixation Rod, 2.5mm FDA UDI
- Model / Reference
- RNL251005 FDA UDI
- Description
- Intramedullary Fixation Rod, 2.5mm FDA UDI
Identifiers
- Catalog Number
- RNL-251-005 FDA UDI
- Primary DI / UDI-DI
- M734RNL2510050 FDA UDI
- FDA Product Code
- HSB FDA UDI
- GMDN Term
- Tibia 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
No
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
Yes
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: Tibia nail, non-sterile
Renovolife Llc by Renovo Life, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Stainless Steel Tibial Nailing System — Orthofix, Inc. · Class II
- Stainless Steel Tibial Nailing System — Orthofix, Inc. · Class II
- AIM™DYNAMIC TIBIAL NAIL — Biomet Orthopedics, Inc. · Class II
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 |
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Manufacturer
- Manufacturer
- Renovo Life, LLC
Sources (1)
- FDA UDI f354f82e-5995-4ee4-aea1-afe23f0050a6 35 fields · synced Jun 1, 2026