Identity
- Trade Name
- INBONE FDA UDI
- Generic Name
- Ankle prosthesis trial, reusable FDA UDI
- Model / Reference
- IB206510 FDA UDI
Identifiers
- Catalog Number
- IB206510 FDA UDI
- Primary DI / UDI-DI
- 00889797048651 FDA UDI
- FDA Product Code
- HSN FDA UDI
- GMDN Term
- Ankle prosthesis trial, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3110 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Height — 10 Millimeter FDA UDI
Category: Ankle prosthesis trial, reusable
Inbone by Wright Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ankle prosthesis trial, reusable.
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- Cadence™ — Ascension Orthopedics, Inc. · Class I
- XT Revision Ankle Replacement System — Smith & Nephew, Inc. · Class I
- Salto Talaris® — Ascension Orthopedics, Inc. · Class I
- Vantage — Exactech, Inc. · Class I
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
- Wright Medical Technology, Inc.
Sources (1)
- FDA UDI 85ef1d6e-51d6-4e2f-9503-aac395b221ab 35 fields · synced Jun 8, 2026