Identity
- Trade Name
- UKNEE Femoral component,non-porous coated FDA UDI
- Generic Name
- Cruciate-retaining total knee prosthesis FDA UDI
- Device Name
- UKNEE Femoral component,non-porous coated,#4,large,left FDA UDI
- Model / Reference
- 2101-1140-B FDA UDI
- Description
- UKNEE Femoral component,non-porous coated,#4,large,left FDA UDI
Identifiers
- Catalog Number
- 2101-1140-B FDA UDI
- Primary DI / UDI-DI
- 04712602345194 FDA UDI
- 510(k) Number
- K021657 FDA UDI
- FDA Product Code
- JWH FDA UDI
- GMDN Term
- Cruciate-retaining total knee prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3560 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cruciate-retaining total knee prosthesis
UKNEE Femoral component, non-porous coated by United Orthopedic Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cruciate-retaining total knee prosthesis.
- Arthrex® — Arthrex, Inc. · Class II
- Columbus® UC — AESCULAP, INC. · Class II
- Optimotion Blue CR HCCR Total Knee System — OPTIMOTION IMPLANTS, LLC · Class II
- B-P TOTAL KNEE SYSTEM — ENDOTEC, INC. · Class II
- DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
- DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
- DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
- DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
Cleared under the same submission
K021657 also covers:
- UKNEE Femoral component, non-porous coated — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, non-porous coated — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, non-porous coated — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, non-porous coated — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, non-porous coated — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, porous coated — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, porous coated — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, porous coated — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, porous coated — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, porous coated — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, posterior stabilized — UNITED ORTHOPEDIC CORP.
- UKNEE Femoral component, posterior stabilized — UNITED ORTHOPEDIC CORP.
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
- United Orthopedic Corp.
Sources (1)
- FDA UDI 1f78451d-79bf-4a1a-aa41-d36256adf5d7 37 fields · synced May 30, 2026