FDA UDI In Commercial Distribution 🇺🇸 United States

U2 Total Knee System

DI: 04719886896459 · Model: 2403-5660 · UNITED ORTHOPEDIC CORP.
Product Codes
3
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
U2 Total Knee System
Primary DI
04719886896459
Version / Model
2403-5660
Catalog Number
2403-5660
Company Name
UNITED ORTHOPEDIC CORP.
Labeler DUNS
656700556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-15
Public Version
1
Public Version Date
2025-09-23
Public Version Status
New
Public Device Record Key
b41e0ab7-a08a-4417-bb0d-299fc2b10c93

Device Description

Patella, Asymmetric Onset, E-XPE, PF+, XX-large, 41×44mm Dia. 11mm Thick

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

GMDN Terms

Code Name
33664 Cruciate-retaining total knee prosthesis
33665 Posterior-stabilized total knee prosthesis
33692 Rotating hinged total knee prosthesis

Identifiers

Type ID
Primary 04719886896459

Customer Contacts