FDA UDI In Commercial Distribution 🇺🇸 United States

USTAR II Knee System

DI: 04719886910902 · Model: 9415-5106 · UNITED ORTHOPEDIC CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
USTAR II Knee System
Primary DI
04719886910902
Version / Model
9415-5106
Catalog Number
9415-5106
Company Name
UNITED ORTHOPEDIC CORP.
Labeler DUNS
656700556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-13
Public Version
1
Public Version Date
2025-11-21
Public Version Status
New
Public Device Record Key
268b0865-2491-483a-ade1-765bdc5ec4cb

Device Description

USTAR II Tibial baseplate driver, XS

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
HWR Driver, Prosthesis

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 04719886910902

Customer Contacts