FDA UDI In Commercial Distribution 🇺🇸 United States

U2 Total Knee System

DI: 04719886903676 · Model: 2403-6430 · UNITED ORTHOPEDIC CORP.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
U2 Total Knee System
Primary DI
04719886903676
Version / Model
2403-6430
Catalog Number
2403-6430
Company Name
UNITED ORTHOPEDIC CORP.
Labeler DUNS
656700556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-11
Public Version
1
Public Version Date
2025-09-19
Public Version Status
New
Public Device Record Key
6f218f2c-743c-447d-b6fa-f8d7f53e4484

Device Description

Patellar trial, onset, NON-CEM, M

Device Characteristics

Single Use
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

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

GMDN Terms

Code Name
58714 Patella prosthesis trial

Identifiers

Type ID
Primary 04719886903676

Customer Contacts