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U2 Femoral component, CR, porous coated

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
U2 Femoral component, CR, porous coated FDA UDI
Generic Name
Cruciate-retaining total knee prosthesis FDA UDI
Device Name
U2 Femoral component, CR, porous coated, #4, left FDA UDI
Model / Reference
2103-1140 FDA UDI
Description
U2 Femoral component, CR, porous coated, #4, left FDA UDI

Identifiers

Catalog Number
2103-1140 FDA UDI
Primary DI / UDI-DI
04712602345392 FDA UDI
510(k) Number
K140075 FDA UDI
FDA Product Code
MBH FDA UDI
GMDN Term
Cruciate-retaining total knee prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3565 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: Posterior-stabilized total knee prosthesisCruciate-retaining total knee prosthesis

U2 Femoral component, CR, 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 925574c2-8ba6-4d4c-89f0-fd1fe7282e44 37 fields · synced Jun 1, 2026