FDA UDI In Commercial Distribution 🇺🇸 United States

U2 Total Knee System

DI: 04719886896442 · Model: 2403-5650 · UNITED ORTHOPEDIC CORP.
Product Codes
3
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
U2 Total Knee System
Primary DI
04719886896442
Version / Model
2403-5650
Catalog Number
2403-5650
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
3fed65d3-32f1-4816-800b-363bf394d5c6

Device Description

Patella, Asymmetric Onset, E-XPE, PF+, X-large, 38×42mm 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 04719886896442

Customer Contacts