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United Hip System, U-Motion II XPE Cup Liner

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
United Hip System, U-Motion II XPE Cup Liner FDA UDI
Generic Name
Ceramic-on-polyethylene total hip prosthesis FDA UDI
Device Name
U-Motion II XPE Cup Liner, 0 DEG., I.D. 32mm, O.D. 78mm FDA UDI
Model / Reference
1406-3278 FDA UDI
Description
U-Motion II XPE Cup Liner, 0 DEG., I.D. 32mm, O.D. 78mm FDA UDI

Identifiers

Catalog Number
1406-3278 FDA UDI
Primary DI / UDI-DI
04712771503753 FDA UDI
510(k) Number
K122185 FDA UDI
FDA Product Code
LZO FDA UDI
MEH FDA UDI
KWY FDA UDI
LWJ FDA UDI
GMDN Term
Ceramic-on-polyethylene total hip prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3390 FDA UDI
888.3360 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

Dimensions & Sizes

Size
Angle — 0 degree FDA UDI
Lumen/Inner Diameter — 32 Millimeter FDA UDI
Outer Diameter — 78 Millimeter FDA UDI

Category: Ceramic-on-polyethylene total hip prosthesisCeramic-on-ceramic total hip prosthesis

United Hip System, U-Motion II XPE Cup Liner by United Orthopedic Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ceramic-on-ceramic total hip 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 54a29368-b7bc-46b1-bb03-18178803a0cb 37 fields · synced May 29, 2026