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U2 Femoral component, CR, porous coated

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 2103-1210

by United Orthopedic Corp.

Identity

Trade Name
U2 Total Knee System EUDAMED
U2 Femoral component, CR, porous coated FDA UDI
Generic Name
Cruciate-retaining total knee prosthesis FDA UDI
Device Name
U2 Total Knee System Femoral Component, Cruciate Retaining, Porous Coated, #1, Right EUDAMED
U2 Femoral component, CR, porous coated, #1, right FDA UDI
Model / Reference
2103-1210 EUDAMEDFDA UDI
Description
U2 Femoral component, CR, porous coated, #1, right FDA UDI

Identifiers

Catalog Number
2103-1210 FDA UDI
Primary DI / UDI-DI
04712602345422 EUDAMEDFDA UDI
Basic UDI-DI
B-04712602345422 EUDAMED
510(k) Number
K140075 FDA UDI
FDA Product Code
MBH FDA UDI
EMDN Code
P0909030102 BICOMPARTMENTAL PRIMARY IMPLANT UNCEMENTED FEMORAL COMPONENTS EUDAMED
GMDN Term
Cruciate-retaining total knee prosthesis FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
888.3565 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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 — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cruciate-retaining total knee prosthesis.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI c779726d-b63f-4877-82fa-c152126b90db 37 fields · synced Oct 7, 2026
  • EUDAMED 2a316f32-00a3-471f-a4ed-8f2c42fbff85 61 fields · synced Oct 7, 2026